Uniform films for rapid-dissolve dosage form incorporating anti-tacking compositions

ABSTRACT

The present invention relates to water-soluble films incorporating anti-tacking agents and methods of their preparation. Anti-tacking agents may improve the flow characteristics of the compositions and thereby reduce the problem of film adhering to a user&#39;s mouth or to other units of film. In particular, the present invention relates to edible water-soluble delivery systems in the form of a film composition including a water-soluble polymer, an active component selected from cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof and at least one anti-tacking agent.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of U.S. ProvisionalApplication No. 60/715,528, filed Sep. 9, 2005, and is acontinuation-in-part of U.S. application Ser. No. 10/074,272, filed Feb.14, 2002, which claims the benefit of U.S. Provisional Application No.60/328,868, filed Oct. 12, 2001, the contents all of which areincorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to rapidly dissolving films incorporatinganti-tacking agents and methods of their preparation. The films also maycontain an active ingredient that is evenly distributed throughout thefilm.

BACKGROUND OF THE RELATED TECHNOLOGY

Active ingredients, such as drugs or pharmaceuticals, may be prepared ina tablet form to allow for accurate and consistent dosing. However, thisform of preparing and dispensing medications has many disadvantagesincluding that a large proportion of adjuvants that must be added toobtain a size able to be handled, that a larger medication form requiresadditional storage space, and that dispensing includes counting thetablets which has a tendency for inaccuracy. In addition, many persons,estimated to be as much as 28% of the population, have difficultyswallowing tablets. While tablets may be broken into smaller pieces oreven crushed as a means of overcoming swallowing difficulties, this isnot a suitable solution for many tablet or pill forms. For example,crushing or destroying the tablet or pill form to facilitate ingestion,alone or in admixture with food, may also destroy the controlled releaseproperties.

As an alternative to tablets and pills, films may be used to carryactive ingredients such as drugs, pharmaceuticals, and the like.However, historically films and the process of making drug deliverysystems therefrom have suffered from a number of unfavorablecharacteristics that have not allowed them to be used in practice.

Films that incorporate a pharmaceutically active ingredient aredisclosed in expired U.S. Pat. No. 4,136,145 to Fuchs, et al. (“Fuchs”).These films may be formed into a sheet, dried and then cut intoindividual doses. The Fuchs disclosure alleges the fabrication of auniform film, which includes the combination of water-soluble polymers,surfactants, flavors, sweeteners, plasticizers and drugs. Theseallegedly flexible films are disclosed as being useful for oral, topicalor enteral use. Examples of specific uses disclosed by Fuchs includeapplication of the films to mucosal membrane areas of the body,including the mouth, rectal, vaginal, nasal and ear areas.

Examination of films made in accordance with the process disclosed inFuchs, however, reveals that such films suffer from the aggregation orconglomeration of particles, i.e., self-aggregation, making theminherently non-uniform. This result can be attributed to Fuchs' processparameters, which although not disclosed likely include the use ofrelatively long drying times, thereby facilitating intermolecularattractive forces, convection forces, air flow and the like to form suchagglomeration.

The formation of agglomerates randomly distributes the film componentsand any active present as well. When large dosages are involved, a smallchange in the dimensions of the film would lead to a large difference inthe amount of active per film. If such films were to include low dosagesof active, it is possible that portions of the film may be substantiallydevoid of any active. Since sheets of film are usually cut into unitdoses, certain doses may therefore be devoid of or contain aninsufficient amount of active for the recommended treatment. Failure toachieve a high degree of accuracy with respect to the amount of activeingredient in the cut film can be harmful to the patient. For thisreason, dosage forms formed by processes such as Fuchs, would not likelymeet the stringent standards of governmental or regulatory agencies,such as the U.S. Federal Drug Administration (“FDA”), relating to thevariation of active in dosage forms. Currently, as required by variousworld regulatory authorities, dosage forms may not vary more than 10% inthe amount of active present. When applied to dosage units based onfilms, this virtually mandates that uniformity in the film be present.

The problems of self-aggregation leading to non-uniformity of a filmwere addressed in U.S. Pat. No. 4,849,246 to Schmidt (“Schmidt”).Schmidt specifically pointed out that the methods disclosed by Fuchs didnot provide a uniform film and recognized that that the creation of anon-uniform film necessarily prevents accurate dosing, which asdiscussed above is especially important in the pharmaceutical area.Schmidt abandoned the idea that a mono-layer film, such as described byFuchs, may provide an accurate dosage form and instead attempted tosolve this problem by forming a multi-layered film. Moreover, hisprocess is a multi-step process that adds expense and complexity and isnot practical for commercial use.

Other U.S. Patents directly addressed the problems of particleself-aggregation and non-uniformity inherent in conventional filmforming techniques. In one attempt to overcome non-uniformity, U.S. Pat.No. 5,629,003 to Horstmann et al. and U.S. Pat. No. 5,948,430 to Zerbeet al. incorporated additional ingredients, i.e. gel formers andpolyhydric alcohols respectively, to increase the viscosity of the filmprior to drying in an effort to reduce aggregation of the components inthe film. These methods have the disadvantage of requiring additionalcomponents, which translates to additional cost and manufacturing steps.Furthermore, both methods employ the use the conventional time-consumingdrying methods such as a high-temperature air-bath using a drying oven,drying tunnel, vacuum drier, or other such drying equipment. The longlength of drying time aids in promoting the aggregation of the activeand other adjuvant, notwithstanding the use of viscosity modifiers. Suchprocesses also run the risk of exposing the active, i.e., a drug, orvitamin C, or other components to prolonged exposure to moisture andelevated temperatures, which may render it ineffective or even harmful.

In addition to the concerns associated with degradation of an activeduring extended exposure to moisture, the conventional drying methodsthemselves are unable to provide uniform films. The length of heatexposure during conventional processing, often referred to as the “heathistory”, and the manner in which such heat is applied, have a directeffect on the formation and morphology of the resultant film product.Uniformity is particularly difficult to achieve via conventional dryingmethods where a relatively thicker film, which is well-suited for theincorporation of a drug active, is desired. Thicker uniform films aremore difficult to achieve because the surfaces of the film and the innerportions of the film do not experience the same external conditionssimultaneously during drying. Thus, observation of relatively thickfilms made from such conventional processing shows a non-uniformstructure caused by convection and intermolecular forces and requiresgreater than 10% moisture to remain flexible. The amount of freemoisture can often interfere over time with the drug leading to potencyissues and therefore inconsistency in the final product.

Conventional drying methods generally include the use of forced hot airusing a drying oven, drying tunnel, and the like. The difficulty inachieving a uniform film is directly related to the rheologicalproperties and the process of water evaporation in the film-formingcomposition. When the surface of an aqueous polymer solution iscontacted with a high temperature air current, such as a film-formingcomposition passing through a hot air oven, the surface water isimmediately evaporated forming a polymer film or skin on the surface.This seals the remainder of the aqueous film-forming composition beneaththe surface, forming a barrier through which the remaining water mustforce itself as it is evaporated in order to achieve a dried film. Asthe temperature outside the film continues to increase, water vaporpressure builds up under the surface of the film, stretching the surfaceof the film, and ultimately ripping the film surface open allowing thewater vapor to escape. As soon as the water vapor has escaped, thepolymer film surface reforms, and this process is repeated, until thefilm is completely dried. The result of the repeated destruction andreformation of the film surface is observed as a “ripple effect” whichproduces an uneven, and therefore non-uniform film. Frequently,depending on the polymer, a surface will seal so tightly that theremaining water is difficult to remove, leading to very long dryingtimes, higher temperatures, and higher energy costs.

Other factors, such as mixing techniques, also play a role in themanufacture of a pharmaceutical film suitable for commercialization andregulatory approval. Air can be trapped in the composition during themixing process or later during the film making process, which can leavevoids in the film product as the moisture evaporates during the dryingstage. The film frequently collapse around the voids resulting in anuneven film surface and therefore, non-uniformity of the final filmproduct. Uniformity is still affected even if the voids in the filmcaused by air bubbles do not collapse. This situation also provides anon-uniform film in that the spaces, which are not uniformlydistributed, are occupying area that would otherwise be occupied by thefilm composition. None of the above-mentioned patents either addressesor proposes a solution to the problems caused by air that has beenintroduced to the film.

Moreover, films go through numerous processing steps prior to primarypackaging, e.g., in canisters, and secondary packaging, e.g., in pouchesor blister packs. The processing steps present significant challengesfor the development of quality films that possess optimal film surfaceproperties such as low coefficient of friction or high slip. Throughoutthis process, it is important to maintain the integrity of the film frominitial manufacture to final packaging. It is desirable, therefore, toprevent or alleviate problems that diminish the integrity of the film,such as films that soften, get tacky, adhere, dry up, or become brittleover time.

More specifically, over-the-counter film products, such as candy andbreath films, typically are packaged in canisters containing 16 filmunits, also referred to as strips, or higher (up to 24 or even 32 filmstrips per canister). The number of film strips per canister variesbased on product type, active dose and packaging configuration amongother considerations. When packaging multiple film strips in a canister,however, problems such as strips sticking to one another often arise.

Adherence between film strips is a common problem encountered in ediblefilm products and may arise due to a variety of reasons. For instance,in some cases, adherence between film strips may be caused by thecomponents used in film manufacture. Components such as flavors,plasticizers, and actives in the film can sometimes soften the film andhave a detrimental effect on film quality. For example, in films havinghigh acidulent content, the acids may exert an excessive plasticizingeffect on the film. Such effect may be intensified by the hygroscopicityof some acids or other components in the film.

In some cases, adherence between film strips may be caused by changes infilm properties due to temperature and/or humidity changes. Some filmsmay become tacky over time when exposed to non-optimal temperatureand/or humidity conditions. This problem may be amplified for productsthat have a very narrow optimal temperature and/or humidity range forstorage.

Overall, films that exhibit tackiness or become tacky over time maypresent numerous problems. First, conversion of master rolls to daughterrolls, and further conversion to film strips becomes substantially moredifficult when film is tacky. In addition, tacky film strips tend toadhere to one another when stacked in packaging, e.g., a canister.Accordingly, it becomes difficult for a user to remove a single filmstrip at a time from the film packaging. Overall, such adherence withinthe packaging decreases the aesthetics of the film strips as well as anindividual consumer's ease of use.

Therefore, there is a need for compositions that enable films to slideagainst one another, thereby providing ease of conversion, maximumstorage stability and ease of consumer use, among other benefits.Further, there is a need for methods of preparing such films, whichmaintain the uniform distribution of components therein, therebypreventing undesired aggregations and promoting uniformity in the finalfilm product.

SUMMARY OF THE INVENTION

In one aspect of the present invention, there is provided an edible filmfor delivery of an active including: an edible, water-soluble polymer;at least one anti-tacking agent selected from the group consisting oflubricants, antiadherants, glidants and combinations thereof; and anactive component selected from the group consisting of cosmetic agents,pharmaceutical agents, vitamins, bioactive agents and combinationsthereof, wherein the film is self-supporting.

In another aspect of the present invention, there is provided an ediblefilm for delivery of an active including: an edible, water-solublepolymer component which includes at least one polymer selected fromhydroxypropyl cellulose, hydroxypropylmethyl cellulose, polyethyleneoxide and combinations thereof; an active component selected fromcosmetic agents, pharmaceutical agents, vitamins, bioactive agents andcombinations thereof; and an anti-tacking agent containing Vitamin ETPGS present in amounts of about 0.01% to about 20% by weight of thefilm.

In another aspect of the present invention, there is provided an ediblefilm for delivery of an active including: an edible, water-solublepolymer component which includes polyethylene oxide in combination witha polymer selected from hydroxypropyl cellulose, hydroxypropylmethylcellulose and combinations thereof; and Vitamin E TPGS present inamounts sufficient to provide anti-tacking and therapeutic properties,wherein the film is self-supporting.

In some embodiments, there is provided an edible film for delivery of anactive which includes: an edible, water-soluble polymer includingpolyethylene oxide and hydroxypropyl cellulose; polydextrose, whereinthe polyethylene oxide, hydroxypropyl cellulose and polydextrose arepresent in a ratio of about 45:45:10; an active component selected fromcosmetic agents, pharmaceutical agents, vitamins, bioactive agents andcombinations thereof; and at least one anti-tacking agent.

In another aspect, there is provided an edible film for delivery of anactive including: (a) a self-supporting film having at least onesurface, the film including: (i) an edible, water-soluble polymer; and(ii) an active component selected from cosmetic agents, pharmaceuticalagents, vitamins, bioactive agents and combinations thereof; and (b) acoating on the at least one surface of the self-supporting film, thecoating including at least one anti-tacking agent.

Some embodiments provide a multi-layer film for delivery of an activeincluding: (a) at least one first film layer containing: (i) an edible,water-soluble polymer; and (ii) an anti-tacking agent; and (b) a secondfilm layer including: (i) an edible, water-soluble polymer; and (ii) anactive component selected from cosmetic agents, pharmaceutical agents,vitamins, bioactive agents and combinations thereof. The first filmlayer is substantially in contact with the second film layer.

The present invention also provides a process for making aself-supporting film having a substantially uniform distribution ofcomponents including the steps of: combining an edible, water-solublepolymer, a solvent, an active component selected from cosmetic agents,pharmaceutical agents, vitamins, bioactive agents and combinationsthereof and at least one anti-tacking agent to form a matrix with auniform distribution of the components; forming a self-supporting filmfrom the matrix; providing a surface having top and bottom sides;feeding the film onto the top side of the surface; and drying the filmby applying heat to the bottom side of the surface.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a side view of a package containing a unit dosage film ofthe present invention.

FIG. 2 shows a top view of two adjacently coupled packages containingindividual unit dosage forms of the present invention, separated by atearable perforation.

FIG. 3 shows a side view of the adjacently coupled packages of FIG. 2arranged in a stacked configuration.

FIG. 4 shows a perspective view of a dispenser for dispensing thepackaged unit dosage forms, dispenser containing the packaged unitdosage forms in a stacked configuration.

FIG. 5 is a schematic view of a roll of coupled unit dose packages ofthe present invention.

FIG. 6 is a schematic view of an apparatus suitable for preparation of apre-mix, addition of an active, and subsequent formation of the film.

FIG. 7 is a schematic view of an apparatus suitable for drying the filmsof the present invention.

DETAILED DESCRIPTION OF THE INVENTION

For the purposes of the present invention the term non-self-aggregatinguniform heterogeneity refers to the ability of the films of the presentinvention, which are formed from one or more components in addition to apolar solvent, to provide a substantially reduced occurrence of, i.e.little or no, aggregation or conglomeration of components within thefilm as is normally experienced when films are formed by conventionaldrying methods such as a high-temperature air-bath using a drying oven,drying tunnel, vacuum drier, or other such drying equipment. The termheterogeneity, as used in the present invention, includes films thatwill incorporate a single component, such as a polymer, as well ascombinations of components, such as a polymer and an active. Uniformheterogeneity includes the substantial absence of aggregates orconglomerates as is common in conventional mixing and heat dryingmethods used to form films.

Furthermore, the films of the present invention have a substantiallyuniform thickness, which is also not provided by the use of conventionaldrying methods used for drying water-based polymer systems. The absenceof a uniform thickness detrimentally affects uniformity of componentdistribution throughout the area of a given film.

The film products of the present invention are produced by a combinationof a properly selected polymer and a polar solvent, optionally includingan active ingredient as well as other fillers known in the art. Thesefilms provide a non-self-aggregating uniform heterogeneity of thecomponents within them by utilizing a selected casting or depositionmethod and a controlled drying process. Examples of controlled dryingprocesses include, but are not limited to, the use of the apparatusdisclosed in U.S. Pat. No. 4,631,837 to Magoon (“Magoon”), hereinincorporated by reference, as well as hot air impingement across thebottom substrate and bottom heating plates. Another drying technique forobtaining the films of the present invention is controlled radiationdrying, in the absence of uncontrolled air currents, such as infraredand radio frequency radiation (i.e. microwaves).

The objective of the drying process is to provide a method of drying thefilms that avoids complications, such as the noted “rippling” effect,that are associated with conventional drying methods and which initiallydry the upper surface of the film, trapping moisture inside. Inconventional oven drying methods, as the moisture trapped insidesubsequently evaporates, the top surface is altered by being ripped openand then reformed. These complications are avoided by the presentinvention, and a uniform film is provided by drying the bottom surfaceof the film first or otherwise preventing the formation of polymer filmformation (skin) on the top surface of the film prior to drying thedepth of the film. This may be achieved by applying heat to the bottomsurface of the film with substantially no top air flow, or alternativelyby the introduction of controlled microwaves to evaporate the water orother polar solvent within the film, again with substantially no top airflow. Yet alternatively, drying may be achieved by using balanced fluidflow, such as balanced air flow, where the bottom and top air flows arecontrolled to provide a uniform film. In such a case, the air flowdirected at the top of the film should not create a condition whichwould cause movement of particles present in the wet film, due to forcesgenerated by the air currents. Additionally, air currents directed atthe bottom of the film should desirably be controlled such that the filmdoes not lift up due to forces from the air. Uncontrolled air currents,either above or below the film, can create non-uniformity in the finalfilm products. The humidity level of the area surrounding the topsurface may also be appropriately adjusted to prevent premature closureor skinning of the polymer surface.

This manner of drying the films provides several advantages. Among theseare the faster drying times and a more uniform surface of the film, aswell as uniform distribution of components for any given area in thefilm. In addition, the faster drying time allows viscosity to quicklybuild within the film, further encouraging a uniform distribution ofcomponents and decrease in aggregation of components in the final filmproduct. Desirably, the drying of the film will occur within about tenminutes or fewer, or more desirably within about five minutes or fewer.

The present invention yields exceptionally uniform film products whenattention is paid to reducing the aggregation of the compositionalcomponents. By avoiding the introduction of and eliminating excessiveair in the mixing process, selecting polymers and solvents to provide acontrollable viscosity and by drying the film in a rapid manner from thebottom up, such films result.

The products and processes of the present invention rely on theinteraction among various steps of the production of the films in orderto provide films that substantially reduce the self-aggregation of thecomponents within the films. Specifically, these steps include theparticular method used to form the film, making the composition mixtureto prevent air bubble inclusions, controlling the viscosity of the filmforming composition and the method of drying the film. Moreparticularly, a greater viscosity of components in the mixture isparticularly useful when the active is not soluble in the selected polarsolvent in order to prevent the active from settling out. However, theviscosity must not be too great as to hinder or prevent the chosenmethod of casting, which desirably includes reverse roll coating due toits ability to provide a film of substantially consistent thickness.

In addition to the viscosity of the film or film-forming components ormatrix, there are other considerations taken into account by the presentinvention for achieving desirable film uniformity. For example, stablesuspensions are achieved which prevent solid (such as drug particles)sedimentation in non-colloidal applications. One approach provided bythe present invention is to balance the density of the particulate(ρ_(p)) and the liquid phase (ρ₁) and increase the viscosity of theliquid phase (μ). For an isolated particle, Stokes law relates theterminal settling velocity (Vo) of a rigid spherical body of radius (r)in a viscous fluid, as follows:V _(o)=(2gr ^(r)) (ρ_(p)−ρ₁)/9μ.

At high particle concentrations, however, the local particleconcentration will affect the local viscosity and density. The viscosityof the suspension is a strong function of solids volume fraction, andparticle-particle and particle-liquid interactions will further hindersettling velocity.

Stokian analyses has shown that the incorporation of a third phase,dispersed air or nitrogen, for example, promotes suspension stability.Further, increasing the number of particles leads to a hindered settlingeffect based on the solids volume fraction. In dilute particlesuspensions, the rate of sedimentation, v, can be expressed as:v/V _(o)=1/(1+κφ)where κ=a constant, and φ is the volume fraction of the dispersed phase.More particles suspended in the liquid phase results in decreasedvelocity. Particle geometry is also an important factor since theparticle dimensions will affect particle-particle flow interactions.

Similarly, the viscosity of the suspension is dependent on the volumefraction of dispersed solids. For dilute suspensions of non-interactionspherical particles, an expression for the suspension viscosity can beexpressed as:μ/μ_(o)=1+2.5φwhere μ_(o) is the viscosity of the continuous phase and φ is the solidsvolume fraction. At higher volume fractions, the viscosity of thedispersion can be expressed asμ/μ_(o)=1+2.5φ+C ₁φ² +C ₂φ³+ . . .where C is a constant.

The viscosity of the liquid phase is critical and is desirably modifiedby customizing the liquid composition to a viscoelastic non-Newtonianfluid with low yield stress values. This is the equivalent of producinga high viscosity continuous phase at rest. Formation of a viscoelasticor a highly structured fluid phase provides additional resistive forcesto particle sedimentation. Further, flocculation or aggregation can becontrolled minimizing particle-particle interactions. The net effectwould be the preservation of a homogeneous dispersed phase.

The addition of hydrocolloids to the aqueous phase of the suspensionincreases viscosity, may produce viscoelasticity and can impartstability depending on the type of hydrocolloid, its concentration andthe particle composition, geometry, size, and volume fraction. Theparticle size distribution of the dispersed phase needs to be controlledby selecting the smallest realistic particle size in the high viscositymedium, i.e., <500 μm. The presence of a slight yield stress or elasticbody at low shear rates may also induce permanent stability regardlessof the apparent viscosity. The critical particle diameter can becalculated from the yield stress values. In the case of isolatedspherical particles, the maximum shear stress developed in settlingthrough a medium of given viscosity can be given asτ_(max)=3Vμ/2r.For pseudoplastic fluids, the viscosity in this shear stress regime maywell be the zero shear rate viscosity at the Newtonian plateau.

A stable suspension is an important characteristic for the manufactureof a pre-mix composition which is to be fed into the film castingmachinery film, as well as the maintenance of this stability in the wetfilm stage until sufficient drying has occurred to lock-in the particlesand matrix into a sufficiently solid form such that uniformity ismaintained. For viscoelastic fluid systems, a rheology that yieldsstable suspensions for extended time period, such as 24 hours, must bebalanced with the requirements of high-speed film casting operations. Adesirable property for the films is shear thinning or pseudoplasticity,whereby the viscosity decreases with increasing shear rate. Timedependent shear effects such as thixotropy are also advantageous.Structural recovery and shear thinning behavior are importantproperties, as is the ability for the film to self-level as it isformed.

The rheology requirements for the inventive compositions and films arequite severe. This is due to the need to produce a stable suspension ofparticles, for example 30-60 wt %, in a viscoelastic fluid matrix withacceptable viscosity values throughout a broad shear rate range. Duringmixing, pumping, and film casting, shear rates in the range of 10-10⁵sec.⁻¹ may be experienced and pseudoplasticity is the preferredembodiment.

In film casting or coating, rheology is also a defining factor withrespect to the ability to form films with the desired uniformity. Shearviscosity, extensional viscosity, viscoelasticity, structural recoverywill influence the quality of the film. As an illustrative example, theleveling of shear-thinning pseudoplastic fluids has been derived asα^((n−1/n))=α_(o) ^((n−1/n))−((n−1)/(2n−1))(τ/K)^(1/n)(2π/λ)^((3+n)/n) h^((2n+1)/n) twhere α is the surface wave amplitude, α_(o) is the initial amplitude, λis the wavelength of the surface roughness, and both “n” and “K” areviscosity power law indices. In this example, leveling behavior isrelated to viscosity, increasing as n decreases, and decreasing withincreasing K.

Desirably, the films or film-forming compositions of the presentinvention have a very rapid structural recovery, i.e. as the film isformed during processing, it doesn't fall apart or become discontinuousin its structure and compositional uniformity. Such very rapidstructural recovery retards particle settling and sedimentation.Moreover, the films or film-forming compositions of the presentinvention are desirably shear-thinning pseudoplastic fluids. Such fluidswith consideration of properties, such as viscosity and elasticity,promote thin film formation and uniformity.

Thus, uniformity in the mixture of components depends upon numerousvariables. As described herein, viscosity of the components, the mixingtechniques and the rheological properties of the resultant mixedcomposition and wet casted film are important aspects of the presentinvention. Additionally, control of particle size and particle shape arefurther considerations. Desirably, the size of the particulate aparticle size of 150 microns or less, for example 100 microns or less.Moreover, such particles may be spherical, substantially spherical, ornon-spherical, such as irregularly shaped particles or ellipsoidallyshaped particles. Ellipsoidally shaped particles or ellipsoids aredesirable because of their ability to maintain uniformity in the filmforming matrix as they tend to settle to a lesser degree as compared tospherical particles.

A number of techniques may be employed in the mixing stage to preventbubble inclusions in the final film. To provide a composition mixturewith substantially no air bubble formation in the final product,anti-foaming or surface-tension reducing agents are employed.Additionally, the speed of the mixture is desirably controlled toprevent cavitation of the mixture in a manner which pulls air into themix. Finally, air bubble reduction can further be achieved by allowingthe mix to stand for a sufficient time for bubbles to escape prior todrying the film. Desirably, the inventive process first forms amasterbatch of film-forming components without active ingredients suchas drug particles or volatile materials such as flavor oils. The activesare added to smaller mixes of the masterbatch just prior to casting.Thus, the masterbatch pre-mix can be allowed to stand for a longer timewithout concern for instability in drug or other ingredients.

When the matrix is formed including the film-forming polymer and polarsolvent in addition to any additives and the active ingredient, this maybe done in a number of steps. For example, the ingredients may all beadded together or a pre-mix may be prepared. The advantage of a pre-mixis that all ingredients except for the active may be combined inadvance, with the active added just prior to formation of the film. Thisis especially important for actives that may degrade with prolongedexposure to water, air or another polar solvent.

FIG. 6 shows an apparatus 20 suitable for the preparation of a pre-mix,addition of an active and subsequent formation of a film. The pre-mix ormaster batch 22, which includes the film-forming polymer, polar solvent,and any other additives except a drug active is added to the masterbatch feed tank 24. The components for pre-mix or master batch 22 aredesirably formed in a mixer (not shown) prior to their addition into themaster batch feed tank 24. Then a pre-determined amount of the masterbatch is controllably fed via a first metering pump 26 and control valve28 to either or both of the first and second mixers, 30, 30′. Thepresent invention, however, is not limited to the use of two mixers, 30,30′, and any number of mixers may suitably be used. Moreover, thepresent invention is not limited to any particular sequencing of themixers 30, 30′, such as parallel sequencing as depicted in FIG. 6, andother sequencing or arrangements of mixers, such as series orcombination of parallel and series, may suitably be used. The requiredamount of the drug or other ingredient, such as a flavor, is added tothe desired mixer through an opening, 32, 32′, in each of the mixers,30, 30′. Desirably, the residence time of the pre-mix or master batch 22is minimized in the mixers 30, 30′. While complete dispersion of thedrug into the pre-mix or master batch 22 is desirable, excessiveresidence times may result in leaching or dissolving of the drug,especially in the case for a soluble drug. Thus, the mixers 30, 30′areoften smaller, i.e. lower residence times, as compared to the primarymixers (not shown) used in forming the pre-mix or master batch 22. Afterthe drug has been blended with the master batch pre-mix for a sufficienttime to provide a uniform matrix, a specific amount of the uniformmatrix is then fed to the pan 36 through the second metering pumps, 34,34′. The metering roller 38 determines the thickness of the film 42 andapplies it to the application roller. The film 42 is finally formed onthe substrate 44 and carried away via the support roller 46.

While the proper viscosity uniformity in mixture and stable suspensionof particles, and casting method are important in the initial steps offorming the composition and film to promote uniformity, the method ofdrying the wet film is also important. Although these parameters andproperties assist uniformity initially, a controlled rapid dryingprocess ensures that the uniformity will be maintained until the film isdry.

The wet film is then dried using controlled bottom drying or controlledmicrowave drying, desirably in the absence of external air currents orheat on the top (exposed) surface of the film 48 as described herein.Controlled bottom drying or controlled microwave drying advantageouslyallows for vapor release from the film without the disadvantages of theprior art. Conventional convection air drying from the top is notemployed because it initiates drying at the top uppermost portion of thefilm, thereby forming a barrier against fluid flow, such as theevaporative vapors, and thermal flow, such as the thermal energy fordrying. Such dried upper portions serve as a barrier to further vaporrelease as the portions beneath are dried, which results in non-uniformfilms. As previously mentioned some top air flow can be used to aid thedrying of the films of the present invention, but it must not create acondition that would cause particle movement or a rippling effect in thefilm, both of which would result in non-uniformity. If top air isemployed, it is balanced with the bottom air drying to avoidnon-uniformity and prevent film lift-up on the carrier belt. A balancetop and bottom air flow may be suitable where the bottom air flowfunctions as the major SOURSce of drying and the top air flow is theminor SOURSce of drying. The advantage of some top air flow is to movethe exiting vapors away from the film thereby aiding in the overalldrying process. The use of any top air flow or top drying, however, mustbe balanced by a number of factors including, but not limited, torheological properties of the composition and mechanical aspects of theprocessing. Any top fluid flow, such as air, also must not overcome theinherent viscosity of the film-forming composition. In other words, thetop air flow cannot break, distort or otherwise physically disturb thesurface of the composition. Moreover, air velocities are desirably belowthe yield values of the film, i.e., below any force level that can movethe liquids in the film-forming compositions. For thin or low viscositycompositions, low air velocity must be used. For thick or high viscositycompositions, higher air velocities may be used. Furthermore, airvelocities are desirable low so as to avoid any lifting or othermovement of the film formed from the compositions.

Moreover, the films of the present invention may contain particles thatare sensitive to temperature, such as flavors, which may be volatile, ordrugs, which may have a low degradation temperature. In such cases, thedrying temperature may be decreased while increasing the drying time toadequately dry the uniform films of the present invention. Furthermore,bottom drying also tends to result in a lower internal film temperatureas compared to top drying. In bottom drying, the evaporating vapors morereadily carry heat away from the film as compared to top drying whichlowers the internal film temperature. Such lower internal filmtemperatures often result in decreased drug degradation and decreasedloss of certain volatiles, such as flavors.

Furthermore, particles or particulates may be added to the film-formingcomposition or matrix after the composition or matrix is cast into afilm. For example, particles may be added to the film 42 prior to thedrying of the film 42. Particles may be controllably metered to the filmand disposed onto the film through a suitable technique, such as throughthe use of a doctor blade (not shown) which is a device which marginallyor softly touches the surface of the film and controllably disposes theparticles onto the film surface. Other suitable, but non-limiting,techniques include the use of an additional roller to place theparticles on the film surface, spraying the particles onto the filmsurface, and the like. The particles may be placed on either or both ofthe opposed film surfaces, i.e., the top and/or bottom film surfaces.Desirably, the particles are securably disposed onto the film, such asbeing embedded into the film. Moreover, such particles are desirably notfully encased or fully embedded into the film, but remain exposed to thesurface of the film, such as in the case where the particles arepartially embedded or partially encased.

The particles may be any useful organoleptic agent, cosmetic agent,pharmaceutical agent, or combinations thereof. Desirably, thepharmaceutical agent is a taste-masked or a controlled-releasepharmaceutical agent. Useful organoleptic agents include flavors andsweeteners. Useful cosmetic agents include breath freshening ordecongestant agents, such as menthol, including menthol crystals.

Although the inventive process is not limited to any particularapparatus for the above-described desirable drying, one particularuseful drying apparatus 50 is depicted in FIG. 7. Drying apparatus 50 isa nozzle arrangement for directing hot fluid, such as but not limited tohot air, towards the bottom of the film 42 which is disposed onsubstrate 44. Hot air enters the entrance end 52 of the drying apparatusand travels vertically upward, as depicted by vectors 54, towards airdeflector 56. The air deflector 56 redirects the air movement tominimize upward force on the film 42. As depicted in FIG. 7, the air istangentially directed, as indicated by vectors 60 and 60′, as the airpasses by air deflector 56 and enters and travels through chamberportions 58 and 58′ of the drying apparatus 50. With the hot air flowbeing substantially tangential to the film 42, lifting of the film as itis being dried is thereby minimized. While the air deflector 56 isdepicted as a roller, other devices and geometries for deflecting air orhot fluid may suitable be used. Furthermore, the exit ends 62 and 62′ ofthe drying apparatus 50 are flared downwardly. Such downward flaringprovides a downward force or downward velocity vector, as indicated byvectors 64 and 64′, which tend to provide a pulling or drag effect ofthe film 42 to prevent lifting of the film 42. Lifting of the film 42may not only result in non-uniformity in the film or otherwise, but mayalso result in non-controlled processing of the film 42 as the film 42and/or substrate 44 lift away from the processing equipment.

Monitoring and control of the thickness of the film also contributes tothe production of a uniform film by providing a film of uniformthickness. The thickness of the film may be monitored with gauges suchas Beta Gauges. A gauge may be coupled to another gauge at the end ofthe drying apparatus, i.e. drying oven or tunnel, to communicate throughfeedback loops to control and adjust the opening in the coatingapparatus, resulting in control of uniform film thickness.

The film products are generally formed by combining a properly selectedpolymer and polar solvent, as well as any active ingredient or filler asdesired. Desirably, the solvent content of the combination is at leastabout 30% by weight of the total combination. The matrix formed by thiscombination is formed into a film, desirably by roll coating, and thendried, desirably by a rapid and controlled drying process to maintainthe uniformity of the film, more specifically, a non-self-aggregatinguniform heterogeneity. The resulting film will desirably contain lessthan about 10% by weight solvent, more desirably less than about 8% byweight solvent, even more desirably less than about 6% by weight solventand most desirably less than about 2%. The solvent may be water, a polarorganic solvent including, but not limited to, ethanol, isopropanol,acetone, methylene chloride, or any combination thereof.

Consideration of the above discussed parameters, such as but not limitedto rheology properties, viscosity, mixing method, casting method anddrying method, also impact material selection for the differentcomponents of the present invention. Furthermore, such considerationwith proper material selection provides the compositions of the presentinvention, including a pharmaceutical and/or cosmetic dosage form orfilm product having no more than a 10% variance of a pharmaceuticaland/or cosmetic active per unit area. In other words, the uniformity ofthe present invention is determined by the presence of no more than a10% by weight of pharmaceutical and/or cosmetic variance throughout thematrix. Desirably, the variance is less than 5% by weight, less than 2%by weight, less than 1% by weight, or less than 0.5% by weight.

Film-Forming Polymers

The polymer may be water soluble, water swellable, water insoluble, or acombination of one or more either water soluble, water swellable orwater insoluble polymers. The polymer may include cellulose or acellulose derivative. Specific examples of useful water soluble polymersinclude, but are not limited to, polyethylene oxide (PEO), pullulan,hydroxypropylmethyl cellulose, hydroxyethyl cellulose, hydroxypropylcellulose, polyvinyl pyrrolidone, carboxymethyl cellulose, polyvinylalcohol, sodium aginate, polyethylene glycol, xanthan gum, tragancanthgum, guar gum, acacia gum, arabic gum, polyacrylic acid,methylmethacrylate copolymer, carboxyvinyl copolymers, starch, gelatin,and combinations thereof. In some embodiments, combinations of PEO and acellulosic polymer, such as hydroxypropyl cellulose, are employed.Specific examples of useful water insoluble polymers include, but arenot limited to, ethyl cellulose, hydroxypropyl ethyl cellulose,cellulose acetate phthalate, hydroxypropyl methyl cellulose phthalateand combinations thereof.

As used herein the phrase “water soluble polymer” and variants thereofrefer to a polymer that is at least partially soluble in water, anddesirably fully or predominantly soluble in water, or absorbs water.Polymers that absorb water are often referred to as being waterswellable polymers. The materials useful with the present invention maybe water soluble or water swellable at room temperature and othertemperatures, such as temperatures exceeding room temperature. Moreover,the materials may be water soluble or water swellable at pressures lessthan atmospheric pressure. Desirably, the water soluble polymers arewater soluble or water swellable having at least 20 percent by weightwater uptake. Water swellable polymers having a 25 or greater percent byweight water uptake are also useful. Films or dosage forms of thepresent invention formed from such water soluble polymers are desirablysufficiently water soluble to be dissolvable upon contact with bodilyfluids.

Other polymers useful for incorporation into the films of the presentinvention include biodegradable polymers, copolymers, block polymers andcombinations thereof. Among the known useful polymers or polymer classeswhich meet the above criteria are: poly(glycolic acid) (PGA),poly(lactic acid) (PLA), polydioxanoes, polyoxalates, poly(α-esters),polyanhydrides, polyacetates, polycaprolactones, poly(orthoesters),polyamino acids, polyaminocarbonates, polyurethanes, polycarbonates,polyamides, poly(alkyl cyanoacrylates), and mixtures and copolymersthereof. Additional useful polymers include, stereopolymers of L-andD-lactic acid, copolymers of bis(p-carboxyphenoxy) propane acid andsebacic acid, sebacic acid copolymers, copolymers of caprolactone,poly(lactic acid)/poly(glycolic acid)/polyethyleneglycol copolymers,copolymers of polyurethane and (poly(lactic acid), copolymers ofpolyurethane and poly(lactic acid), copolymers of α-amino acids,copolymers of α-amino acids and caproic acid, copolymers of α-benzylglutamate and polyethylene glycol, copolymers of succinate andpoly(glycols), polyphosphazene, polyhydroxy-alkanoates and mixturesthereof. Binary and ternary systems are contemplated.

Other specific polymers useful include those marketed under the Medisorband Biodel trademarks. The Medisorb materials are marketed by the DupontCompany of Wilmington, Delaware and are generically identified as a“lactide/glycolide co-polymer” containing “propanoic acid,2-hydroxy-polymer with hydroxy-polymer with hydroxyacetic acid.” Foursuch polymers include lactide/glycolide 100L, believed to be 100%lactide having a melting point within the range of 338°-347° F.(170°-175° C.); lactide/glycolide 100L, believed to be 100% glycolidehaving a melting point within the range of 437°-455° F. (225°-235° C.);lactide/glycolide 85/15, believed to be 85% lactide and 15% glycolidewith a melting point within the range of 338°-347° F. (170°-175° C.);and lactide/glycolide 50/50, believed to be a copolymer of 50% lactideand 50% glycolide with a melting point within the range of 338°-347° F.(170°-175° C.).

The Biodel materials represent a family of various polyanhydrides whichdiffer chemically.

Although a variety of different polymers may be used, it is desired toselect polymers to provide a desired viscosity of the mixture prior todrying. For example, if the active or other components are not solublein the selected solvent, a polymer that will provide a greater viscosityis desired to assist in maintaining uniformity. On the other hand, ifthe components are soluble in the solvent, a polymer that provides alower viscosity may be preferred.

The polymer plays an important role in affecting the viscosity of thefilm. Viscosity is one property of a liquid that controls the stabilityof the active in an emulsion, a colloid or a suspension. Generally theviscosity of the matrix will vary from about 400 cps to about 100,000cps, preferably from about 800 cps to about 60,000 cps, and mostpreferably from about 1,000 cps to about 40,000 cps. Desirably, theviscosity of the film-forming matrix will rapidly increase uponinitiation of the drying process.

The viscosity may be adjusted based on the selected active depending onthe other components within the matrix. For example, if the component isnot soluble within the selected solvent, a proper viscosity may beselected to prevent the component from settling which would adverselyaffect the uniformity of the resulting film. The viscosity may beadjusted in different ways. To increase viscosity of the film matrix,the polymer may be chosen of a higher molecular weight or crosslinkersmay be added, such as salts of calcium, sodium and potassium. Theviscosity may also be adjusted by adjusting the temperature or by addinga viscosity increasing component. Components that will increase theviscosity or stabilize the emulsion/suspension include higher molecularweight polymers and polysaccharides and gums, which include withoutlimitation, alginate, carrageenan, hydroxypropyl methyl cellulose,locust bean gum, guar gum, xanthan gum, dextran, gum arabic, gellan gumand combinations thereof.

It has also been observed that certain polymers which when used alonewould ordinarily require a plasticizer to achieve a flexible film, canbe combined without a plasticizer and yet achieve flexible films. Forexample, HPMC and HPC when used in combination provide a flexible,strong film with the appropriate plasticity and elasticity formanufacturing and storage. No additional plasticizer or polyalcohol isneeded for flexibility.

Controlled Release Films

The term “controlled release” is intended to mean the release of activeat a pre-selected or desired rate. This rate will vary depending uponthe application. Desirable rates include fast or immediate releaseprofiles as well as delayed, sustained or sequential release.Combinations of release patterns, such as initial spiked releasefollowed by lower levels of sustained release of active arecontemplated. Pulsed drug releases are also contemplated.

The polymers that are chosen for the films of the present invention mayalso be chosen to allow for controlled disintegration of the active.This may be achieved by providing a substantially water insoluble filmthat incorporates an active that will be released from the film overtime. This may be accomplished by incorporating a variety of differentsoluble or insoluble polymers and may also include biodegradablepolymers in combination. Alternatively, coated controlled release activeparticles may be incorporated into a readily soluble film matrix toachieve the controlled release property of the active inside thedigestive system upon consumption.

Films that provide a controlled release of the active are particularlyuseful for buccal, gingival, sublingual and vaginal applications. Thefilms of the present invention are particularly useful where mucosalmembranes or mucosal fluid is present due to their ability to readilywet and adhere to these areas.

The convenience of administering a single dose of a medication whichreleases active ingredients in a controlled fashion over an extendedperiod of time as opposed to the administration of a number of singledoses at regular intervals has long been recognized in thepharmaceutical arts. The advantage to the patient and clinician inhaving consistent and uniform blood levels of medication over anextended period of time are likewise recognized. The advantages of avariety of sustained release dosage forms are well known. However, thepreparation of a film that provides the controlled release of an activehas advantages in addition to those well-known for controlled releasetablets. For example, thin films are difficult to inadvertently aspirateand provide an increased patient compliance because they need not beswallowed like a tablet. Moreover, certain embodiments of the inventivefilms are designed to adhere to the buccal cavity and tongue, where theycontrollably dissolve. Furthermore, thin films may not be crushed in themanner of controlled release tablets which is a problem leading to abuseof drugs such as Oxycontin.

The actives employed in the present invention may be incorporated intothe film compositions of the present invention in a controlled releaseform. For example, particles of drug may be coated with polymers such asethyl cellulose or polymethacrylate, commercially available under brandnames such as Aquacoat ECD and Eudragit E-100, respectively. Solutionsof drug may also be absorbed on such polymer materials and incorporatedinto the inventive film compositions. Other components such as fats andwaxes, as well as sweeteners and/or flavors may also be employed in suchcontrolled release compositions.

The actives may be taste-masked prior to incorporation into the filmcomposition, as set forth in co-pending PCT application titled, UniformFilms For Rapid Dissolve Dosage Form Incorporating Taste-MaskingCompositions, (based on U.S. Provisional Application No. Express MailLabel No.: EU552991605 US of the same title, filed Sep. 27, 2003,attorney docket No. 1199-15P) the entire subject matter of which isincorporated by reference herein.

Actives

When an active is introduced to the film, the amount of active per unitarea is determined by the uniform distribution of the film. For example,when the films are cut into individual dosage forms, the amount of theactive in the dosage form can be known with a great deal of accuracy.This is achieved because the amount of the active in a given area issubstantially identical to the amount of active in an area of the samedimensions in another part of the film. The accuracy in dosage isparticularly advantageous when the active is a medicament, i.e. a drug.

The active components that may be incorporated into the films of thepresent invention include, without limitation pharmaceutical andcosmetic actives, drugs, medicaments, antigens or allergens such asragweed pollen, spores, microorganisms including bacteria, seeds,mouthwash components such as chlorates or chlorites, flavors,fragrances, enzymes, preservatives, sweetening agents, colorants,spices, vitamins and combinations thereof.

A wide variety of medicaments, bioactive active substances andpharmaceutical compositions may be included in the dosage forms of thepresent invention. Examples of useful drugs include ace-inhibitors,antianginal drugs, anti-arrhythmias, anti-asthmatics,anti-cholesterolemics, analgesics, anesthetics, anti-convulsants,anti-depressants, anti-diabetic agents, anti-diarrhea preparations,antidotes, anti-histamines, anti-hypertensive drugs, anti-inflammatoryagents, anti-lipid agents, anti-manics, anti-nauseants, anti-strokeagents, anti-thyroid preparations, anti-tumor drugs, anti-viral agents,acne drugs, alkaloids, amino acid preparations, anti-tussives,anti-uricemic drugs, anti-viral drugs, anabolic preparations, systemicand non-systemic anti-infective agents, anti-neoplastics,anti-parkinsonian agents, anti-rheumatic agents, appetite stimulants,biological response modifiers, blood modifiers, bone metabolismregulators, cardiovascular agents, central nervous system stimulates,cholinesterase inhibitors, contraceptives, decongestants, dietarysupplements, dopamine receptor agonists, endometriosis managementagents, enzymes, erectile dysfunction therapies, fertility agents,gastrointestinal agents, homeopathic remedies, hormones, hypercalcemiaand hypocalcemia management agents, immunomodulators,immunosuppressives, migraine preparations, motion sickness treatments,muscle relaxants, obesity management agents, osteoporosis preparations,oxytocics, parasympatholytics, parasympathomimetics, prostaglandins,psychotherapeutic agents, respiratory agents, sedatives, smokingcessation aids such as bromocryptine and nicotine, sympatholytics,tremor preparations, urinary tract agents, vasodilators, laxatives,antacids, ion exchange resins, anti-pyretics, appetite suppressants,expectorants, anti-anxiety agents, anti-ulcer agents, anti-inflammatorysubstances, coronary dilators, cerebral dilators, peripheralvasodilators, psycho-tropics, stimulants, anti-hypertensive drugs,vasoconstrictors, migraine treatments, antibiotics, tranquilizers,anti-psychotics, anti-tumor drugs, anti-coagulants, anti-thromboticdrugs, hypnotics, anti-emetics, anti-nauseants, anti-convulsants,neuromuscular drugs, hyper- and hypo-glycemic agents, thyroid andanti-thyroid preparations, diuretics, anti-spasmodics, terine relaxants,anti-obesity drugs, erythropoietic drugs, anti-asthmatics, coughsuppressants, mucolytics, DNA and genetic modifying drugs, andcombinations thereof.

Examples of medicating active ingredients contemplated for use in thepresent invention include antacids, H₂-antagonists, and analgesics. Forexample, antacid dosages can be prepared using the ingredients calciumcarbonate alone or in combination with magnesium hydroxide, and/oraluminum hydroxide. Moreover, antacids can be used in combination withH₂-antagonists.

Analgesics include opiates and opiate derivatives, such as oxycodone(available as Oxycontin®), ibuprofen, aspirin, acetaminophen, andcombinations thereof that may optionally include caffeine.

Other preferred drugs for other preferred active ingredients for use inthe present invention include anti-diarrheals such as immodium AD,anti-histamines, anti-tussives, decongestants, vitamins, and breathfresheners. Suitable vitamins contemplated for use herein include anyconventionally known vitamins, such as, but not limited to, Vitamins A,B, C and E. Common drugs used alone or in combination for colds, pain,fever, cough, congestion, runny nose and allergies, such asacetaminophen, chlorpheniramine maleate, dextromethorphan,pseudoephedrine HCl and diphenhydramine may be included in the filmcompositions of the present invention.

Also contemplated for use herein are anxiolytics such as alprazolam(available as Xanax®); anti-psychotics such as clozopin (available asClozaril®) and haloperidol (available as Haldol®); non-steroidalanti-inflammatories (NSAID's) such as dicyclofenacs (available asVoltaren®) and etodolac (available as Lodine®), anti-histamines such asloratadine (available as Claritin®), astemizole (available asHismanal™), nabumetone (available as Relafen®), and Clemastine(available as Tavist®); anti-emetics such as granisetron hydrochloride(available as Kytril®) and nabilone (available as Cesamet™);bronchodilators such as Bentolin®, albuterol sulfate (available asProventil®); anti-depressants such as fluoxetine hydrochloride(available as Prozac®), sertraline hydrochloride (available as Zoloft®),and paroxtine hydrochloride (available as Paxil®); anti-migraines suchas Imigra®, ACE-inhibitors such as enalaprilat (available as Vasotec(®),captopril (available as Capoten(®) and lisinopril (available asZestril®); anti-Alzheimer's agents, such as nicergoline; andCaH-antagonists such as nifedipine (available as Procardia® andAdalat®), and verapamil hydrochloride (available as Calan®).

Erectile dysfunction therapies include, but are not limited to, drugsfor facilitating blood flow to the penis, and for effecting autonomicnervous activities, such as increasing parasympathetic (cholinergic) anddecreasing sympathetic (adrenersic) activities. Useful non-limitingdrugs include sildenafils, such as Viagra®, tadalafils, such as Cialis®,vardenafils, apomorphines, such as Uprima®, yohimbine hydrochloridessuch as Aphrodyne®, and alprostadils such as Caverject®.

The popular H₂-antagonists which are contemplated for use in the presentinvention include cimetidine, ranitidine hydrochloride, famotidine,nizatidien, ebrotidine, mifentidine, roxatidine, pisatidine andaceroxatidine.

Active antacid ingredients include, but are not limited to, thefollowing: aluminum hydroxide, dihydroxyaluminum aminoacetate,aminoacetic acid, aluminum phosphate, dihydroxyaluminum sodiumcarbonate, bicarbonate, bismuth aluminate, bismuth carbonate, bismuthsubcarbonate, bismuth subgallate, bismuth subnitrate, bismuthsubsilysilate, calcium carbonate, calcium phosphate, citrate ion (acidor salt), amino acetic acid, hydrate magnesium aluminate sulfate,magaldrate, magnesium aluminosilicate, magnesium carbonate, magnesiumglycinate, magnesium hydroxide, magnesium oxide, magnesium trisilicate,milk solids, aluminum mono-ordibasic calcium phosphate, tricalciumphosphate, potassium bicarbonate, sodium tartrate, sodium bicarbonate,magnesium aluminosilicates, tartaric acids and salts.

The pharmaceutically active agents employed in the present invention mayinclude allergens or antigens, such as, but not limited to, plantpollens from grasses, trees, or ragweed; animal danders, which are tinyscales shed from the skin and hair of cats and other furred animals;insects, such as house dust mites, bees, and wasps; and drugs, such aspenicillin.

Botanicals, herbals and minerals also may be added to the film. Examplesof botanicals include, without limitation: roots; barks; leaves; stems;flowers; fruits; tobacco; sunflower seeds; snuff; and combinationsthereof.

An anti-oxidant may also be added to the film to prevent the degradationof an active, especially where the active is photosensitive.

The bioactive active substances employed in the present invention mayinclude beneficial bacteria. More specifically, certain bacterianormally exist on the surface of the tongue and in the back of thethroat. Such bacteria assist in the digestion of food by breaking downproteins found in the food. It may be desirable, therefore, toincorporate these bacteria into the oral film products of the presentinvention.

It also may be desirable to include actives for treating breath malodorand related oral care conditions, such as actives which are effective insuppressing microorganisms. Because breath malodor can be caused by thepresence of anaerobic bacteria in the oral cavity, which generatevolatile sulfur compounds, components that suppress such microorganismsmay be desirable. Examples of such components include antimicrobialssuch as triclosan, chlorine dioxide, chlorates, and chlorites, amongothers. The use of chlorites, particularly sodium chlorite, in oral carecompositions such as mouthrinses and toothpastes is taught in U.S. Pat.Nos. 6,251,372, 6,132,702, 6,077,502, and U.S. Publication No.2003/0129144, all of which are incorporated herein by reference. Suchcomponents are incorporated in amounts effective to treat malodor andrelated oral conditions.

Cosmetic active agents may include breath freshening compounds likementhol, other flavors or fragrances, especially those used for oralhygiene, as well as actives used in dental and oral cleansing such asquaternary ammonium bases. The effect of flavors may be enhanced usingflavor enhancers like tartaric acid, citric acid, vanillin, or the like.

Also color additives can be used in preparing the films. Such coloradditives include food, drug and cosmetic colors (FD&C), drug andcosmetic colors (D&C), or external drug and cosmetic colors (Ext. D&C).These colors are dyes, their corresponding lakes, and certain naturaland derived colorants. Lakes are dyes absorbed on aluminum hydroxide.

Other examples of coloring agents include known azo dyes, organic orinorganic pigments, or coloring agents of natural origin. Inorganicpigments are preferred, such as the oxides or iron or titanium, theseoxides, being added in concentrations ranging from about 0.001 to about10%, and preferably about 0.5 to about 3%, based on the weight of allthe components.

Flavors may be chosen from natural and synthetic flavoring liquids. Anillustrative list of such agents includes volatile oils, syntheticflavor oils, flavoring aromatics, oils, liquids, oleoresins or extractsderived from plants, leaves, flowers, fruits, stems and combinationsthereof. A non-limiting representative list of examples includes mintoils, cocoa, and citrus oils such as lemon, orange, grape, lime andgrapefruit and fruit essences including apple, pear, peach, grape,strawberry, raspberry, cherry, plum, pineapple, apricot or other fruitflavors.

The films containing flavorings may be added to provide a hot or coldflavored drink or soup. These flavorings include, without limitation,tea and soup flavorings such as beef and chicken.

Other useful flavorings include aldehydes and esters such asbenzaldehyde (cherry, almond), citral i.e., alphacitral (lemon, lime),neral, i.e., beta-citral (lemon, lime), decanal (orange, lemon),aldehyde C-8 (citrus fruits), aldehyde C-9 (citrus fruits), aldehydeC-12 (citrus fruits), tolyl aldehyde (cherry, almond),2,6-dimethyloctanol (green fruit), and 2-dodecenal (citrus, mandarin),combinations thereof and the like.

The sweeteners may be chosen from the following non-limiting list:glucose (corn syrup), dextrose, invert sugar, fructose, and combinationsthereof; saccharin and its various salts such as the sodium salt;dipeptide sweeteners such as aspartame; dihydrochalcone compounds,glycyrrhizin; Stevia Rebaudiana (Stevioside); chloro derivatives ofsucrose such as sucralose; sugar alcohols such as sorbitol, mannitol,xylitol, and the like. Also contemplated are hydrogenated starchhydrolysates and the synthetic sweetener3,6-dihydro-6-methyl-1-1-1,2,3-oxathiazin-4-one-2,2-dioxide,particularly the potassium salt (acesulfame-K), and sodium and calciumsalts thereof, and natural intensive sweeteners, such as Lo Han Kuo.Other sweeteners may also be used.

When the active is combined with the polymer in the solvent, the type ofmatrix that is formed depends on the solubilities of the active and thepolymer. If the active and/or polymer are soluble in the selectedsolvent, this may form a solution. However, if the components are notsoluble, the matrix may be classified as an emulsion, a colloid, or asuspension.

Dosages

The film products of the present invention are capable of accommodatinga wide range of amounts of the active ingredient. The films are capableof providing an accurate dosage amount (determined by the size of thefilm and concentration of the active in the original polymer/watercombination) regardless of whether the required dosage is high orextremely low. Therefore, depending on the type of active orpharmaceutical composition that is incorporated into the film, theactive amount may be as high as about 300 mg, desirably up to about 150mg or as low as the microgram range, or any amount therebetween.

The film products and methods of the present invention are well suitedfor high potency, low dosage drugs. This is accomplished through thehigh degree of uniformity of the films. Therefore, low dosage drugs,particularly more potent racemic mixtures of actives are desirable.

Anti-tacking Compositions

It is useful to add anti-tacking agents, such as lubricants,antiadherants and glidants to the film compositions of the presentinvention. Anti-tacking agents assist in the flow characteristics of thematerial, for example, by reducing sticking to the die in extrusionprocesses and reducing sticking to the roof of the mouth duringadministration of the dosage form.

During consumption of films, particles tend to adhere to the roof of themouth. This is undesirable for films containing bitter drugs, such as,for example, dextromethorphan, because the adhered particles elude drug,which increases the amount of bitterness detected by the user. Additionof an anti-tacking agent to the films reduces adherence to the roof ofthe mouth, thereby effectively reducing the bitterness that may bedetected by a user during consumption.

Anti-taking agents also may impart reduced film-to-film coefficient offriction, thereby reducing the problem of film dosage units, i.e.,strips, adhering to one another. More specifically, in many types offilm packaging, strips are stacked against one another. Theincorporation of anti-tacking agents may permit the individual strips toslide smoothly against one another as each unit is removed from thepackaging.

Examples of suitable lubricants for use as anti-tacking agents include,but are not limited to: stearates, such as magnesium stearate, calciumstearate, and sodium stearate; stearic acid; sterotex; talc; waxes;stearowet; boric acid; sodium benzoate; sodium acetate; sodium chloride;DL-Leucine; Carbowax 4000; Carbowax 6000; sodium oleate; sodium laurylsulfate; magnesium lauryl sulfate; and combinations thereof.

Examples of suitable antiadherants include, but are not limited to:talc; cornstarch; Cab-O-Sil; syloid; DL-Leucine; sodium lauryl sulfate;metallic stearates; and combinations thereof. Examples of suitableglidants include, but are not limited to: talc; cornstarch; Cab-O-Sil;syloid; aerosol; and combinations thereof.

Some embodiments of the present invention include fats and/or waxes asanti-tacking agents.

Vitamin E is another suitable anti-tacking agent for use in someembodiments of the present invention. Vitamin E may serve as both ananti-tacking agent and an active component in the film. Desirably,Vitamin E TPGS (d-alpha tocopheryl polyethylene glycol 1000 succinate)is employed. Vitamin E TPGS is a water-soluble form of Vitamin E derivedfrom natural sources. As compared to other forms, Vitamin E TPGS iseasily absorbed. Further, Vitamin E TPGS imparts practically no taste tofilm. Vitamin E TPGS may be employed in solution, such as, for example10% or 20% solution with water. Vitamin E TPGS is particularly useful inreducing the stickiness of the films and the tendency to adhere to theroof of the user's mouth. Vitamin E may be present in amounts of about0.01% to about 20% by weight of the composition.

Anti-tacking agents generally are present in amounts of about 0.01% toabout 20% by weight of the film composition. More specifically,anti-tacking agents may be present in amounts of about 0.01% to about10% by weight of the film composition, and even more specifically, about0.25% to about 5% by weight of the film composition.

Combinations of anti-tacking agents also may be employed. For instance,in some embodiments of the present invention, a combination of astearate, such as magnesium stearate, and silica may be used. SIPERNAT500LS, which is a silica product having a 4.5 μm mean particle size, issuitable for use herein (commercially available from Degussa).Combinations of magnesium stearate and silica may provide improvedglidant properties, i.e., assist film strips in sliding smoothly againstone another in packaging. Accordingly, in some embodiments, magnesiumstearate may be present in amounts of about 0.1% to about 2.5% by weightof the film composition and silica may be present in amounts of about0.1% to about 1.5% by weight of the film composition. Such combinationof anti-tacking agents may be useful in a variety of films containingdifferent flavors and/or actives.

In some embodiments, anti-tacking agents may be included in the filmcomposition itself. For example, single or multi-layer films includinganti-tacking agents may be formed. Multi-layer films, for example, mayinclude two, three or more layers of film substantially in contact withone another. In some embodiments, the film layers may be laminated toone another. Anti-tacking agents may be present in one or more of thelayers of the multi-layer film. For example, some embodiments mayinclude a bi-layer film in which anti-tacking agents are present in oneof the two film layers. Some embodiments may include a three-layer filmin which anti-tacking agents are present in each of the outer layers butnot in the inner, or middle, layer of the three-layer film. Inaccordance therewith, a variety of different combinations of layers maybe formed.

Alternatively, in some embodiments, anti-tacking agents may be includedin a composition that is used to coat the external surfaces of the film.For instance, anti-tacking agents may be applied to the film in the formof a wet or dry coating, such as, for example, a sugared or sugar-freecoating. The film may be coated with the anti-tacking agents in anyconventional manner, such as, but not limited to, dip coating, spraycoating, dusting, or fluidized bed. One or more film surfaces may becoated. In some embodiments, the anti-tacking coating may be applied toa substrate, such as a backing for the film, rather than directly to thefilm itself. When the film is removed from the backing, the anti-tackingcoating may adhere to the film.

Anti-foaming and De-foaming Compositions

Anti-foaming and/or de-foaming components may also be used with thefilms of the present invention. These components aid in the removal ofair, such as entrapped air, from the film-forming compositions. Asdescribed above, such entrapped air may lead to non-uniform films.Simethicone is one particularly useful anti-foaming and/or de-foamingagent. The present invention, however, is not so limited and otheranti-foam and/or de-foaming agents may suitable be used.

Simethicone is generally used in the medical field as a treatment forgas or colic in babies. Simethicone is a mixture of fully methylatedlinear siloxane polymers containing repeating units ofpolydimethylsiloxane which is stabilized with trimethylsiloxyend-blocking unites, and silicon dioxide. It usually contains 90.5-99%polymethylsiloxane and 4-7% silicon dioxide. The mixture is a gray,translucent, viscous fluid which is insoluble in water.

When dispersed in water, simethicone will spread across the surface,forming a thin film of low surface tension. In this way, simethiconereduces the surface tension of bubbles air located in the solution, suchas foam bubbles, causing their collapse. The function of simethiconemimics the dual action of oil and alcohol in water. For example, in anoily solution any trapped air bubbles will ascend to the surface anddissipate more quickly and easily, because an oily liquid has a lighterdensity compared to a water solution. On the other hand, analcohol/water mixture is known to lower water density as well as lowerthe water's surface tension. So, any air bubbles trapped inside thismixture solution will also be easily dissipated. Simethicone solutionprovides both of these advantages. It lowers the surface energy of anyair bubbles that trapped inside the aqueous solution, as well aslowering the surface tension of the aqueous solution. As the result ofthis unique functionality, simethicone has an excellent anti-foamingproperty that can be used for physiological processes (anti-gas instomach) as well as any for external processes that require the removalof air bubbles from a product.

In order to prevent the formation of air bubbles in the films of thepresent invention, the mixing step can be performed under vacuum.However, as soon as the mixing step is completed, and the film solutionis returned to the normal atmosphere condition, air will bere-introduced into or contacted with the mixture. In many cases, tinyair bubbles will be again trapped inside this polymeric viscoussolution. The incorporation of simethicone into the film-formingcomposition either substantially reduces or eliminates the formation ofair bubbles.

Simethicone may be added to the film-forming mixture as an anti-foamingagent in an amount from about 0.01 weight percent to about 5.0 weightpercent, more desirably from about 0.05 weight percent to about 2.5weight percent, and most desirably from about 0.1 weight percent toabout 1.0 weight percent.

Optional Components

A variety of other components and fillers may also be added to the filmsof the present invention. These may include, without limitation,surfactants; plasticizers which assist in compatibilizing the componentswithin the mixture; polyalcohols; anti-foaming agents, such assilicone-containing compounds, which promote a smoother film surface byreleasing oxygen from the film; and thermo-setting gels such as pectin,carageenan, and gelatin, which help in maintaining the dispersion ofcomponents.

The variety of additives that can be incorporated into the inventivecompositions may provide a variety of different functions. Examples ofclasses of additives include excipients, lubricants, buffering agents,stabilizers, blowing agents, pigments, coloring agents, fillers, bulkingagents, sweetening agents, flavoring agents, fragrances, releasemodifiers, adjuvants, plasticizers, flow accelerators, mold releaseagents, polyols, granulating agents, diluents, binders, buffers,absorbents, glidants, adhesives, anti-adherents, acidulants, softeners,resins, demulcents, solvents, surfactants, emulsifiers, elastomers andmixtures thereof. These additives may be added with the activeingredient(s).

Useful additives include, for example, gelatin, vegetable proteins suchas sunflower protein, soybean proteins, cotton seed proteins, peanutproteins, grape seed proteins, whey proteins, whey protein isolates,blood proteins, egg proteins, acrylated proteins, water-solublepolysaccharides such as alginates, carrageenans, guar gum, agar-agar,xanthan gum, gellan gum, gum arabic and related gums (gum ghatti, gumkaraya, gum tragancanth), pectin, water-soluble derivatives ofcellulose: alkylcelluloses hydroxyalkylcelluloses andhydroxyalkylalkylcelluloses, such as methylcelulose,hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose,hydroxyethylmethylcellulose, hydroxypropylmethylcellulose,hydroxybutylmethylcellulose, cellulose esters and hydroxyalkylcelluloseesters such as cellulose acetate phthalate (CAP),hydroxypropylmethylcellulose (HPMC); carboxyalkylcelluloses,carboxyalkylalkylcelluloses, carboxyalkylcellulose esters such ascarboxymethylcellulose and their alkali metal salts; water-solublesynthetic polymers such as polyacrylic acids and polyacrylic acidesters, polymethacrylic acids and polymethacrylic acid esters,polyvinylacetates, polyvinylalcohols, polyvinylacetatephthalates (PVAP),polyvinylpyrrolidone (PVP), PVY/vinyl acetate copolymer, andpolycrotonic acids; also suitable are phthalated gelatin, gelatinsuccinate, crosslinked gelatin, shellac, water soluble chemicalderivatives of starch, cationically modified acrylates and methacrylatespossessing, for example, a tertiary or quaternary amino group, such asthe diethylaminoethyl group, which may be quaternized if desired; andother similar polymers.

Such extenders may optionally be added in any desired amount desirablywithin the range of up to about 80%, desirably about 3% to 50% and moredesirably within the range of 3% to 20% based on the weight of allcomponents.

Further additives may be inorganic fillers, such as the oxides ofmagnesium aluminum, silicon, titanium, etc. desirably in a concentrationrange of about 0.02% to about 3% by weight and desirably about 0.02% toabout 1% based on the weight of all components.

Further examples of additives are plasticizers which includepolyalkylene oxides, such as polyethylene glycols, polypropyleneglycols, polyethylene-propylene glycols, organic plasticizers with lowmolecular weights, such as glycerol, glycerol monoacetate, diacetate ortriacetate, triacetin, polysorbate, cetyl alcohol, propylene glycol,sorbitol, sodium diethylsulfosuccinate, triethyl citrate, tributylcitrate, and the like, added in concentrations ranging from about 0.5%to about 30%, and desirably ranging from about 0.5% to about 20% basedon the weight of the polymer.

There may further be added compounds to improve the flow properties ofthe starch material such as animal or vegetable fats, desirably in theirhydrogenated form, especially those which are solid at room temperature.These fats desirably have a melting point of 50° C. or higher. Preferredare tri-glycerides with C₁₂-, C₁₄-, C₁₆-, C₁₈-, C₂₀- and C₂₂- fattyacids. These fats can be added alone without adding extenders orplasticizers and can be advantageously added alone or together withmono- and/or di-glycerides or phosphatides, especially lecithin. Themono- and di-glycerides are desirably derived from the types of fatsdescribed above, i.e. with C₁₂-, C₁₄-, C₁₆-, Cl₈-, C₂₀- and C₂₂- fattyacids.

The total amounts used of the fats, mono-, di-glycerides and/orlecithins are up to about 5% and preferably within the range of about0.5% to about 2% by weight of the total composition

It is further useful to add silicon dioxide, calcium silicate, ortitanium dioxide in a concentration of about 0.02% to about 1% by weightof the total composition. These compounds act as texturizing agents.

These additives are to be used in amounts sufficient to achieve theirintended purpose. Generally, the combination of certain of theseadditives will alter the overall release profile of the activeingredient and can be used to modify, i.e. impede or accelerate therelease.

Lecithin is one surface active agent for use in the present invention.Lecithin can be included in the feedstock in an amount of from about0.25% to about 2.00% by weight. Other surface active agents, i.e.surfactants, include, but are not limited to, cetyl alcohol, sodiumlauryl sulfate, the Spans™ and Tweens™ which are commercially availablefrom ICI Americas, Inc. Ethoxylated oils, including ethoxylated castoroils, such as Cremophor® EL which is commercially available from BASF,are also useful. Carbowax™ is yet another modifier which is very usefulin the present invention. Tweens™ or combinations of surface activeagents may be used to achieve the desired hydrophilic-lipophilic balance(“HLB”). The present invention, however, does not require the use of asurfactant and films or film-forming compositions of the presentinvention may be essentially free of a surfactant while still providingthe desirable uniformity features of the present invention.

It may be further useful to add polydextrose to the films of the presentinvention. Polydextrose serves as a filler and solubility enhancer,i.e., it increases the dissolution time of the films in the oral cavity.

As additional modifiers which enhance the procedure and product of thepresent invention are identified, Applicants intend to include all suchadditional modifiers within the scope of the invention claimed herein.

Other ingredients include binders which contribute to the ease offormation and general quality of the films. Non-limiting examples ofbinders include starches, pregelatinize starches, gelatin,polyvinylpyrrolidone, methylcellulose, sodium carboxymethylcellulose,ethylcellulose, polyacrylamides, polyvinyloxoazolidone, andpolyvinylalcohols.

Forming the Film

The films of the present invention must be formed into a sheet prior todrying. After the desired components are combined to form amulti-component matrix, including the polymer, water, and an active orother components as desired, the combination is formed into a sheet orfilm, by any method known in the art such as extrusion, coating,spreading, casting or drawing the multi-component matrix. If amulti-layered film is desired, this may be accomplished by co-extrudingmore than one combination of components which may be of the same ordifferent composition. A multi-layered film may also be achieved bycoating, spreading, or casting a combination onto an already formed filmlayer.

Although a variety of different film-forming techniques may be used, itis desirable to select a method that will provide a flexible film, suchas reverse roll coating. The flexibility of the film allows for thesheets of film to be rolled and transported for storage or prior tobeing cut into individual dosage forms. Desirably, the films will alsobe self-supporting or in other words able to maintain their integrityand structure in the absence of a separate support. Furthermore, thefilms of the present invention may be selected of materials that areedible or ingestible.

Coating or casting methods are particularly useful for the purpose offorming the films of the present invention. Specific examples includereverse roll coating, gravure coating, immersion or dip coating,metering rod or meyer bar coating, slot die or extrusion coating, gap orknife over roll coating, air knife coating, curtain coating, orcombinations thereof, especially when a multi-layered film is desired.

Roll coating, or more specifically reverse roll coating, is particularlydesired when forming films in accordance with the present invention.This procedure provides excellent control and uniformity of theresulting films, which is desired in the present invention. In thisprocedure, the coating material is measured onto the applicator rollerby the precision setting of the gap between the upper metering rollerand the application roller below it. The coating is transferred from theapplication roller to the substrate as it passes around the supportroller adjacent to the application roller. Both three roll and four rollprocesses are common.

The gravure coating process relies on an engraved roller running in acoating bath, which fills the engraved dots or lines of the roller withthe coating material. The excess coating on the roller is wiped off by adoctor blade and the coating is then deposited onto the substrate as itpasses between the engraved roller and a pressure roller.

Offset Gravure is common, where the coating is deposited on anintermediate roller before transfer to the substrate.

In the simple process of immersion or dip coating, the substrate isdipped into a bath of the coating, which is normally of a low viscosityto enable the coating to run back into the bath as the substrateemerges.

In the metering rod coating process, an excess of the coating isdeposited onto the substrate as it passes over the bath roller. Thewire-wound metering rod, sometimes known as a Meyer Bar, allows thedesired quantity of the coating to remain on the substrate. The quantityis determined by the diameter of the wire used on the rod.

In the slot die process, the coating is squeezed out by gravity or underpressure through a slot and onto the substrate. If the coating is 100%solids, the process is termed “Extrusion” and in this case, the linespeed is frequently much faster than the speed of the extrusion. Thisenables coatings to be considerably thinner than the width of the slot.

The gap or knife over roll process relies on a coating being applied tothe substrate which then passes through a “gap” between a “knife” and asupport roller. As the coating and substrate pass through, the excess isscraped off.

Air knife coating is where the coating is applied to the substrate andthe excess is “blown off” by a powerful jet from the air knife. Thisprocedure is useful for aqueous coatings.

In the curtain coating process, a bath with a slot in the base allows acontinuous curtain of the coating to fall into the gap between twoconveyors. The object to be coated is passed along the conveyor at acontrolled speed and so receives the coating on its upper face.

Drying the Film

The drying step is also a contributing factor with regard to maintainingthe uniformity of the film composition. A controlled drying process isparticularly important when, in the absence of a viscosity increasingcomposition or a composition in which the viscosity is controlled, forexample by the selection of the polymer, the components within the filmmay have an increased tendency to aggregate or conglomerate. Analternative method of forming a film with an accurate dosage, that wouldnot necessitate the controlled drying process, would be to cast thefilms on a predetermined well. With this method, although the componentsmay aggregate, this will not result in the migration of the active to anadjacent dosage form, since each well may define the dosage unit per se.

When a controlled or rapid drying process is desired, this may bethrough a variety of methods. A variety of methods may be used includingthose that require the application of heat. The liquid carriers areremoved from the film in a manner such that the uniformity, or morespecifically, the non-self-aggregating uniform heterogeneity, that isobtained in the wet film is maintained.

Desirably, the film is dried from the bottom of the film to the top ofthe film. Desirably, substantially no air flow is present across the topof the film during its initial setting period, during which a solid,visco-elastic structure is formed. This can take place within the firstfew minutes, e.g. about the first 0.5 to about 4.0 minutes of the dryingprocess. Controlling the drying in this manner, prevents the destructionand reformation of the film's top surface, which results fromconventional drying methods. This is accomplished by forming the filmand placing it on the top side of a surface having top and bottom sides.Then, heat is initially applied to the bottom side of the film toprovide the necessary energy to evaporate or otherwise remove the liquidcarrier. The films dried in this manner dry more quickly and evenly ascompared to air-dried films, or those dried by conventional dryingmeans. In contrast to an air-dried film that dries first at the top andedges, the films dried by applying heat to the bottom dry simultaneouslyat the center as well as at the edges. This also prevents settling ofingredients that occurs with films dried by conventional means.

The temperature at which the films are dried is about 100° C. or less,desirably about 90° C. or less, and most desirably about 80° C. or less.

Another method of controlling the drying process, which may be usedalone or in combination with other controlled methods as disclosed aboveincludes controlling and modifying the humidity within the dryingapparatus where the film is being dried. In this manner, the prematuredrying of the top surface of the film is avoided.

Additionally, it has also been discovered that the length of drying timecan be properly controlled, i.e. balanced with the heat sensitivity andvolatility of the components, and particularly the flavor oils anddrugs. The amount of energy, temperature and length and speed of theconveyor can be balanced to accommodate such actives and to minimizeloss, degradation or ineffectiveness in the final film.

A specific example of an appropriate drying method is that disclosed byMagoon. Magoon is specifically directed toward a method of drying fruitpulp. However, the present inventors have adapted this process towardthe preparation of thin films.

The method and apparatus of Magoon are based on an interesting propertyof water. Although water transmits energy by conduction and convectionboth within and to its surroundings, water only radiates energy withinand to water. Therefore, the apparatus of Magoon includes a surface ontowhich the fruit pulp is placed that is transparent to infraredradiation. The underside of the surface is in contact with a temperaturecontrolled water bath. The water bath temperature is desirablycontrolled at a temperature slightly below the boiling temperature ofwater. When the wet fruit pulp is placed on the surface of theapparatus, this creates a “refractance window.” This means that infraredenergy is permitted to radiate through the surface only to the area onthe surface occupied by the fruit pulp, and only until the fruit pulp isdry. The apparatus of Magoon provides the films of the present inventionwith an efficient drying time reducing the instance of aggregation ofthe components of the film.

The films may initially have a thickness of about 500 μm to about 1,500μm, or about 20 mils to about 60 mils, and when dried have a thicknessfrom about 3 μm to about 250 μm, or about 0.1 mils to about 10 mils.Desirably, the dried films will have a thickness of about 2 mils toabout 8 mils, and more desirably, from about 3 mils to about 6 mils.

Uses of Thin Films

The thin films of the present invention are well suited for many uses.The high degree of uniformity of the components of the film makes themparticularly well suited for incorporating pharmaceuticals. Furthermore,the polymers used in construction of the films may be chosen to allowfor a range of disintegration times for the films. A variation orextension in the time over which a film will disintegrate may achievecontrol over the rate that the active is released, which may allow for asustained release delivery system. In addition, the films may be usedfor the administration of an active to any of several body surfaces,especially those including mucous membranes, such as oral, anal,vaginal, ophthalmological, the surface of a wound, either on a skinsurface or within a body such as during surgery, and similar surfaces.

The films may be used to orally administer an active. This isaccomplished by preparing the films as described above and introducingthem to the oral cavity of a mammal. This film may be prepared andadhered to a second or support layer from which it is removed prior touse, i.e. introduction to the oral cavity. An adhesive may be used toattach the film to the support or backing material which may be any ofthose known in the art, and is preferably not water soluble. If anadhesive is used, it will desirably be a food grade adhesive that isingestible and does not alter the properties of the active. Mucoadhesivecompositions are particularly useful. The film compositions in manycases serve as mucoadhesives themselves.

The films may be applied under or to the tongue of the mammal. When thisis desired, a specific film shape, corresponding to the shape of thetongue may be preferred. Therefore the film may be cut to a shape wherethe side of the film corresponding to the back of the tongue will belonger than the side corresponding to the front of the tongue.Specifically, the desired shape may be that of a triangle or trapezoid.Desirably, the film will adhere to the oral cavity preventing it frombeing ejected from the oral cavity and permitting more of the active tobe introduced to the oral cavity as the film dissolves.

Another use for the films of the present invention takes advantage ofthe films' tendency to dissolve quickly when introduce to a liquid. Anactive may be introduced to a liquid by preparing a film in accordancewith the present invention, introducing it to a liquid, and allowing itto dissolve. This may be used either to prepare a liquid dosage form ofan active, or to flavor a beverage.

The films of the present invention are desirably packaged in sealed, airand moisture resistant packages to protect the active from exposureoxidation, hydrolysis, volatilization and interaction with theenvironment. Referring to FIG. 1, a packaged pharmaceutical dosage unit10, includes each film 12 individually wrapped in a pouch or betweenfoil and/or plastic laminate sheets 14. As depicted in FIG. 2, thepouches 10, 10′can be linked together with tearable or perforated joints16. The pouches 10, 10′be packaged in a roll as depicted in FIG. 5 orstacked as shown in FIG. 3 and sold in a dispenser 18 as shown in FIG.4. The dispenser may contain a full supply of the medication typicallyprescribed for the intended therapy, but due to the thinness of the filmand package, is smaller and more convenient than traditional bottlesused for tablets, capsules and liquids. Moreover, the films of thepresent invention dissolve instantly upon contact with saliva or mucosalmembrane areas, eliminating the need to wash the dose down with water.

Desirably, a series of such unit doses are packaged together inaccordance with the prescribed regimen or treatment, e.g., a 10-90 daysupply, depending on the particular therapy. The individual films can bepackaged on a backing and peeled off for use.

The features and advantages of the present invention are more fullyshown by the following examples which are provided for purposes ofillustration, and are not to be construed as limiting the invention inany way.

EXAMPLES Examples 1-2

Water-soluble thin film compositions were prepared using the amountsdescribed in Table 1. In particular, composition 1 incorporated VitaminE as an anti-tacking agent along with various other components.Composition 2 contained similar components to composition 1, but absentVitamin E. TABLE 1 Weight (g unless otherwise indicated) Component 1 2Polyethylene oxide 2.8 3.5 Hydroxypropyl cellulose 2.8 3.5 Polydextrose0.69 0.79 Sucralose 0.35 0.75 Taste-Masking flavor¹ 0.07 0 Titaniumdioxide 0.07 0.18 Coated dextromethorphan (45% w/w) 5.56 6.94 Mintflavor 1.26 1.71 Vitamin E² 3.9 0 WS-3³ 0.035 0.044 Simethiconeemulsion⁴ 0.035 0.09 Water 19.49 32.5 Blue food color 4 drops 5 drops¹Magna Sweet, available from Mafco Worldwide Corp.²10% solution containing 0.39 g Vitamin E and 3.51 g water³N-Ethyl-p-menthane-3-carboxamide cooling agent, available fromMillennium Chemicals⁴Available from Sentry

The above components for each composition were combined by mixing untila uniform mixture was achieved, and then cast into films. In particular,the solutions were cast onto release paper (available from Griff Paper &Film) using a K Control Coater with a 350 micron smooth bar. The filmswere then dried at about 80° C. for about 10 minutes. Composition 1 wasdried to a moisture level of about 2.68%, and composition 2 was dried toa moisture level of about 3.35%.

The dried films were tested for various properties, includingdissolution testing to determine how long it will take the film todissolve in the mouth and bend testing to determine flexibility of thefilm. In addition, a panel observed the tendency of the films to exhibitstickiness in the mouth and the tendency to adhere to the roof of theuser's mouth.

To test dissolution rate, an approximately 20 mm by 100 mm piece offilm, having a 2.85 g weight attached, was lowered into a 32.5° C. waterbath to a depth of about 50 mm. The time required for the film todissolve and separate into two pieces was determined (in seconds).

The films also were subject to bend testing, i.e., 180° bend test. Thedried films were placed in a moisture analyzer (HR73 Moisture Analyzerfrom Mettler Toledo) to obtain percent moisture and to remove anysolvent (e.g. water) remaining in the films after drying at 80° C.accordance with the present invention. The films then were creased toabout 180° and observed for break. Films that broke during creasing wereconsidered a failure. If the film did not break during creasing, a 200 gweight was dropped onto the creased film from a height of about 8.5 mm.Films that broke were considered a failure, and those that did not breakwere considered a pass. It should be noted, however, that thisflexibility test is an extreme test. Films that failed this test arestill considered operable within the scope of the present invention.More specifically, there may be certain applications that do not requiresuch extreme flexibility properties.

Both films of compositions 1 and 2 exhibited adequate strength, goodtear resistance, passed the 180° bend test both prior and subsequent toplacement in the moisture analyzer and dissolved on the tongue at amoderate to fast rate. Composition 1, which contained Vitamin E,exhibited no stickiness in the mouth and did not exhibit a tendency toadhere to the roof of the user's mouth. Composition 2, in contrast, didnot contain Vitamin E. Composition 2 exhibited stickiness and tendencyto adhere to the roof of the mouth.

Examples 3 - 243

Water-soluble thin films were prepared incorporating silica andmagnesium stearate as anti-tacking agents in the amounts described inTable 2. More specifically, various combinations of silica and magnesiumstearate were incorporated into a variety of different film compositionsas shown in the table below. TABLE 2 Magnesium Silica¹ stearate ExampleFilm description (weight %) (weight %) 3 SOURS 1.5 2.0 4 SOURS 1.5 2.0 5SOURS 1.5 2.0 6 SOURS 1.5 2.0 7 SOURS 1.5 2.0 8 SOURS 1.5 2.0 9 SOURS1.5 2.0 10 SOURS 1.5 2.0 11 SOURS 1.5 2.0 12 SOURS 1.5 2.0 13 SOURS 1.52.0 14 SOURS 1.5 2.0 15 BENZOCAINE/MENTHOL 1.5 1.5 16 BENZOCAINE/MENTHOL1.5 1.5 17 BENZOCAINE/MENTHOL 1.5 1.5 18 BENZOCAINE/MENTHOL 1.5 1.5 19BENZOCAINE/MENTHOL 1.5 1.5 20 SOURS 2 2.5 21 SOURS 1.5 2 22 SOURS 1.5 223 SOURS 1.5 2 24 SOURS 1.5 2 25 SOURS 1.5 2 26 SOURS 1.5 2 27 SOURS 1.52.5 28 SOURS 1.5 2.5 29 SOURS 1.5 2.5 30 SOURS 1.5 2.5 31 SOURS 1.5 2 32SOURS 1.5 2 33 SOURS 1.5 2.5 34 SOURS 1.5 2.5 35 SOURS 1.5 2.5 36 SOURS1.5 2.5 37 SOURS 1.5 2.5 38 SOURS 1.5 2.5 39 SOURS 1.5 2.5 40 SOURS 1.52.5 41 ENERGY/WELLNESS SUPPLEMENT² 1 2 42 ENERGY/WELLNESS SUPPLEMENT² 12 43 ENERGY/WELLNESS SUPPLEMENT² 0.9 1 44 ENERGY/WELLNESS SUPPLEMENT²1.15 1 45 ENERGY/WELLNESS SUPPLEMENT² 1 1 46 ENERGY/WELLNESS SUPPLEMENT²0.75 1 47 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 48 ENERGY/WELLNESSSUPPLEMENT² 1 1 49 ENERGY/WELLNESS SUPPLEMENT² 0.75 1 50 ENERGY/WELLNESSSUPPLEMENT² 1 1 51 ENERGY/WELLNESS SUPPLEMENT² 1 1 52 ENERGY/WELLNESSSUPPLEMENT² 1 1 53 ENERGY/WELLNESS SUPPLEMENT² 1 1 54 ENERGY/WELLNESSSUPPLEMENT² 1 1 55 ENERGY/WELLNESS SUPPLEMENT² 1 1 56 ENERGY/WELLNESSSUPPLEMENT² 1 1 57 ENERGY/WELLNESS SUPPLEMENT² 1 1 58 ENERGY/WELLNESSSUPPLEMENT² 1 1 59 ENERGY/WELLNESS SUPPLEMENT² 1 1 60 ENERGY/WELLNESSSUPPLEMENT² 1 1 61 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 62 ENERGY/WELLNESSSUPPLEMENT² 0.5 1.5 63 ORAL ANALGESIC 0.54 0.5 64 ORAL ANALGESIC 1.54 165 ORAL ANALGESIC 0.5 0.54 66 ORAL ANALGESIC 1.54 1 67 ORAL ANALGESIC1.04 1 68 ORAL ANALGESIC 1.24 1.5 69 ORAL ANALGESIC 1.24 1.5 70 ORALANALGESIC 1.24 1.5 71 ORAL ANALGESIC 1.24 1.5 72 ORAL ANALGESIC 1.24 1.573 ORAL ANALGESIC 1.24 1.5 74 ENERGY/WELLNESS SUPPLEMENT² 0.5 1.5 75MELATONIN 1 2 76 MELATONIN 1 2 77 MELATONIN 1 2 78 MELATONIN 1 1.5 79MELATONIN 1.1 1.3 80 MELATONIN 1.2 1.3 81 CHLORINE DIOXIDE 1.5 1.5 82MULTIVITAMIN 1 1 83 MULTIVITAMIN 1 1 84 ZINC/ELDERBERRY 0.5 1 85ENERGY/WELLNESS SUPPLEMENT² 0.75 1 86 ENERGY/WELLNESS SUPPLEMENT² 0.75 187 ENERGY/WELLNESS SUPPLEMENT² 0.75 1 88 MELATONIN 1.1 1.3 89MULTIVITAMIN 1 1 90 B-COMPLEX VITAMIN 1 1 91 MULTIVITAMIN 1 1 92B-COMPLEX VITAMIN 1 1 93 MULTIVITAMIN 1 1 94 MULTIVITAMIN 1 1 95ENERGY/WELLNESS SUPPLEMENT² 0.75 1 96 MULTIVITAMIN 1 1 97 MELATONIN 1 198 ENERGY/WELLNESS SUPPLEMENT² 0.75 1 99 ENERGY/WELLNESS SUPPLEMENT²0.75 1 100 ENERGY/WELLNESS SUPPLEMENT² 0.75 1 101 ENERGY/WELLNESSSUPPLEMENT² 1 1.5 102 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 103ENERGY/WELLNESS SUPPLEMENT² 1 2 104 ENERGY/WELLNESS SUPPLEMENT² 1.5 1105 ENERGY/WELLNESS SUPPLEMENT² 1 2 106 ENERGY/WELLNESS SUPPLEMENT² 1 2107 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 108 ENERGY/WELLNESS SUPPLEMENT² 12 109 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 110 ENERGY/WELLNESS SUPPLEMENT²1 1.5 111 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 112 ENERGY/WELLNESSSUPPLEMENT² 1 1.5 113 ENERGY/WELLNESS SUPPLEMENT² 1 1.5 114ENERGY/WELLNESS SUPPLEMENT² 1 1.5 115 MULTIVITAMIN 1 1.5 116MULTIVITAMIN 1 1.5 117 IMMUNE BOOSTER 1 1 118 MELATONIN 1.1 1.3 119MELATONIN 1.1 1.3 120 MELATONIN 1.1 1.3 121 MELATONIN 1.1 1.3 122MELATONIN 0.5 0.75 123 COLD & COUGH 1 1 124 COLD & COUGH 1 1 125MULTIVITAMIN 1 1 126 MULTIVITAMIN 1 1 127 MULTIVITAMIN 1 1.5 128MULTIVITAMIN 1 1 129 MULTIVITAMIN 1 1 130 MULTIVITAMIN 1 1.5 131MULTIVITAMIN 1 1 132 MULTIVITAMIN 1 1 133 B-COMPLEX VITAMIN 1 1 134B-COMPLEX VITAMIN 1 1 135 B-COMPLEX VITAMIN 1 1 136 B-COMPLEX VITAMIN 11 137 ENERGY/WELLNESS SUPPLEMENT² 1.5 1.5 138 ENERGY/WELLNESSSUPPLEMENT² 1.5 1.5 139 ENERGY/WELLNESS SUPPLEMENT² 1.5 1.5 140MULTIVITAMIN 1 1 141 B-COMPLEX VITAMIN 1 1 142 B-COMPLEX VITAMIN 1 1 143MULTIVITAMIN 1 1 144 B-COMPLEX VITAMIN 1 1 145 MULTIVITAMIN 1 1 146MULTIVITAMIN 1 1 147 MULTIVITAMIN 1 1 148 MULTIVITAMIN 1 1 149 B-COMPLEXVITAMIN 1 1 150 B-COMPLEX VITAMIN 1 1 151 MULTIVITAMIN 1 1 152MULTIVITAMIN 1 1 153 MULTIVITAMIN 1 1 154 MULTIVITAMIN 1.5 0.3 155ENERGY/WELLNESS SUPPLEMENT² 1.5 1 156 ENERGY/WELLNESS SUPPLEMENT² 1 1157 ENERGY/WELLNESS SUPPLEMENT² 1 1 158 MULTIVITAMIN 1 1 159MULTIVITAMIN 1 1 160 MULTIVITAMIN 1.5 0.3 161 MULTIVITAMIN 1 1 162B-COMPLEX VITAMIN 1 1 163 B-COMPLEX VITAMIN 1 1 164 ENERGY/WELLNESSSUPPLEMENT² 0.5 0.5 165 ENERGY/WELLNESS SUPPLEMENT² 0.5 0.5 166ENERGY/WELLNESS SUPPLEMENT² 0.5 0.5 167 ENERGY/WELLNESS SUPPLEMENT² 0.50.5 168 ENERGY/WELLNESS SUPPLEMENT² 0.5 0.5 169 ENERGY/WELLNESSSUPPLEMENT² 0.5 0.5 170 ENERGY/WELLNESS SUPPLEMENT² 0.5 0.5 171ENERGY/WELLNESS SUPPLEMENT² 1 0.5 172 ENERGY/WELLNESS SUPPLEMENT² 1 0.5173 MULTIVITAMIN 1 1 174 MULTIVITAMIN 1 1 175 ENERGY/WELLNESSSUPPLEMENT² 0.5 0.5 176 MULTIVITAMIN 1 1 177 ENERGY/WELLNESS SUPPLEMENT²0.5 0.5 178 ENERGY/WELLNESS SUPPLEMENT² 0.5 0.5 179 MULTIVITAMIN 1 1 180MULTIVITAMIN 1 1 181 ENERGY/WELLNESS SUPPLEMENT² 1 0.5 182ENERGY/WELLNESS SUPPLEMENT² 1 0.5 183 MULTIVITAMIN 1 1 184 MULTIVITAMIN1 1 185 MULTIVITAMIN 1 1 186 MULTIVITAMIN 1 1 187 MULTIVITAMIN 1 1 188ENERGY/WELLNESS SUPPLEMENT² 1 0.5 189 MULTIVITAMIN 1 1 190 MULTIVITAMIN1 1 191 MULTIVITAMIN 1 1 192 MULTLVITAMIN 1 1 193 MULTIVITAMIN 1.37 2.05194 MULTIVITAMIN 1 1 195 MULTIVITAMIN 1 1 196 MULTIVITAMIN 1 1 197B-COMPLEX VITAMIN 1 1 198 ENERGY/WELLNESS SUPPLEMENT² 1 0.5 199ENERGY/WELLNESS SUPPLEMENT² 1 0.5 200 ENERGY/WELLNESS SUPPLEMENT² 1 0.5201 B-COMPLEX VITAMIN 1 1 202 MULTIVITAMIN 1 1 203 MULTIVITAMIN 1 1 204MELATONIN 1.1 1.3 205 MULTIVITAMIN 1.5 0.3 206 MULTLVITAMIN 1 1 207STRESS RELIEF 1 0.3 208 MULTIVITAMIN 1 1 209 MULTIVITAMIN 1 1 210MULTIVITAMIN 1 1 211 ENERGY/WELLNESS SUPPLEMENT² 1 0.5 212ENERGY/WELLNESS SUPPLEMENT² 1 0.5 213 ENERGY/WELLNESS SUPPLEMENT² 1 0.5214 ENERGY/WELLNESS SUPPLEMENT² 1 0.5 215 ENERGY/WELLNESS SUPPLEMENT² 10.5 216 MULTIVITAMIN 1.5 0.3 217 MELATONIN 1 0.5 218 MELATONIN 1 0.5 219STRESS RELIEF 1 0.3 220 MULTIVITAMIN 1 1 221 MELATONIN 1 0.5 222MULTIVITAMIN 1.5 0.3 223 MULTIVITAMIN 1 1 224 MULTIVITAMIN 1 1 225CINNAMINT 1 1 226 MELATONIN 1 0.5 227 MELATONIN 1 0.5 228 B-COMPLEXVITAMIN 1 1 229 MULTIVITAMIN 1 1 230 MULTIVITAMIN 1 1 231 MULTIVITAMIN 11 232 MULTIVITAMIN 1 1 233 MULTIVITAMIN 1 1 234 MULTIVITAMIN 1 1 235MULTIVITAMIN 1 1 236 MULTIVITAMIN 1 1 237 MULTIVITAMIN 1 1 238MULTIVITAMIN 1 1 239 MULTIVITAMIN 1 1 240 MULTIVITAMIN 1 1 241BENZOCAINE/MENTHOL 1.5 1.5 242 MULTIVITAMIN 1 1 243 DEXTROMETHORPHANHYDROBROMIDE 0.5 1.82¹Sipernat 500LS, available from Degussa²Energy/Wellness Supplement may contain any/all of the following activesor combinations thereof: Green Tea, Guarana, Chromium Picolinate,Caffeine, Yohimbie HCl, Taurine, Vitamin B3, Vitamin B6, Vitamin B12

In addition to silica and magnesium stearate, each of the films listedabove contains a variety of components, such as polymers and flavors,among others. The remainder of the components are provided below foreach film description used in Table 2.

Films identified in Table 2 above as “SOURS” contain the followingcomponents listed in Table 3. TABLE 3 Component Weight % HYDROXYPROPYLMETHYLCELLULOSE 0.01%-60% CITRIC ACID 0.01%-40% NATURAL & ARTIFICIALFLAVORS 0.01%-25% GUM ARABIC 0.01%-10% MAGNESIUM STEARATE 0.01%-10%SODIUM HEXAMETAPHOSPHATE 0.01%-5%  SILICA 0.01%-2%  POLYSORBATE 80  0%-5% MALIC ACID 0.01%-10% ASPARTAME  0.01%-3.5% POTASSIUM ACESULFAME 0.01%-0.5% DYE 0.01%-1%  POTASSIUM SORBATE  0.01%-0.1% SODIUM BENZOATE 0.01%-0.1%

Films identified in Table 2 above as “Benzocaine/Menthol” contain thefollowing components listed in Table 4: TABLE 4 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-70% NATURAL & ARTIFICIAL FLAVORS0.01%-25% POLYETHYLENE OXIDE 0.01%-50% MENTHOL CRYSTALS 0.01%-30% CORNSTARCH 0.01%-30% BENZOCAINE 0.01%-10% SUCRALOSE 0.01%-5%  MALIC ACID0.01%-5%  MAGNESIUM STEARATE 0.01%-10% SILICA 0.01%-2%  TITANIUM DIOXIDE0.01%-5%  BUTYLATED HYDROXYTOLUENE 0.01%-1%  DYE 0.01%-1% 

Films identified in Table 2 above as “Energy/Wellness Supplement”contain the following components listed in Table 5: TABLE 5 ComponentWeight % HYDROXYPROPYL METHYLCELLULOSE    0%-70%% HYDROXYPROPYLCELLULOSE 0%-40% PECTIN 0%-40% NATURAL & ARTIFICIAL FLAVORS/FLAVOR0%-30% ADJUVANTS POLYDEXTROSE 0.01%-30%   SODIUM CARBOXYMETHYLCELLULOSE0%-10% ENERGY/WELLNESS ACTIVES² 0.01%-50%   ERYTHRITOL 0%-20% SUCRALOSE0.01%-5%    CITRIC ACID 0%-10% MAGNESIUM STEARATE 0.01%-10%   GLYCERYLMONOOLEATE 0%-1%  SILICA 0.01%-2%    POLYSORBATE 80 0%-1%  SORBITANMONOOLEATE 0%-1%  POTASSIUM SORBATE  0%-0.1% SODIUM BENZOATE  0%-0.1%SODIUM HEXAMETAPHOSPHATE 0%-10% PROPYLENE GLYCOL 0%-25% GUM ARABIC0%-10% DYE 0.01%-1%   

Films identified in Table 2 above as “ORAL ANALGESIC” contain thefollowing components listed in Table 6: TABLE 6 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-70% CHOLINE SALICYLATE 0.01%-60%NATURAL & ARTIFICIAL FLAVORS 0.01%-10% MAGNESIUM STEARATE  0.01-5%SILICA  0.01-2% CETALKONIUM CHLORIDE 0.01%-5%  METHYL PARABEN 0.01%-0.1% DIMETHYLPOLYSILOXANE   0.01%-0.05%

Films identified in Table 2 above as “Melatonin” contain the followingcomponents listed in Table 7: TABLE 7 Component Weight % HYDROXYPROPYLMETHYLCELLULOSE 0.01%-70% NATURAL & ARTIFICIAL FLAVORS/FLAVOR 0.01%-20%ADJUVANTS POLYETHYLENE OXIDE 0.01%-30% MELATONIN 0.01%-20% PECTIN0.01%-10% POLYDEXTROSE 0.01%-20% SUCRALOSE 0.01%-5%  MAGNESIUM STEARATE0.01%-10% SILICA 0.01%-2%  GLYCERYL MONOOLEATE 0.01%-1%  TITANIUMDIOXIDE 0.01%-5%  MONOAMMONIUM GLYCYRRHIZINATE 0.01%-2%  BUTYLATEDHYDROXYTOLUENE 0.01%-1%  DYE 0.01%-1% 

Films identified in Table 2 above as “Chlorine Dioxide” contain thefollowing components listed in Table 8: TABLE 8 Component Weight %HYDROXYPROPYL METHYLCELLULOSE  0.01%-70% POLYETHYLENE OXIDE  0.01%-50%POLYDEXTROSE  0.01%-20% NATURAL & ARTIFICIAL FLAVORS/FLAVOR  0.01%-30%ADJUVANTS MAGNESIUM STEARATE 0.01%-5% SILICA 0.01%-2% SUCRALOSE 0.01%-5%ZINC GLUCONATE DIHYDRATE 0.01%-5% CITRIC ACID 0.01%-2% GLYCERYLMONOOLEATE 0.01%-1% SODIUM HYDROXIDE 0.01%-5% SODIUM BICARBONATE0.01%-5% CHLORINE DIOXIDE 2% SOLUTION  0.01%-10% BUTYLATEDHYDROXYTOLUENE 0.01%-1% DYE 0.01%-1% SODIUM BENZOATE   0.01%-0.1%

Films identified in Table 2 above as “Multivitamin” contain thefollowing components listed in Table 9: TABLE 9 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-50% NATURAL & ARTIFICIAL FLAVORS0.01%-20% NIACINAMIDE - 100% (Vitamin B3) 0.01%-30% POLYETHYLENE OXIDE0.01%-30% POLYDEXTROSE 0.01%-20% ASCORBIC ACID - 100% (Vitamin C)0.01%-20% 50% VITAMIN E ACETATE - 91.2% 0.01%-10% CALCIUMd-PANTOTHENATE - 92% (Vitamin 0.01%-10% B5) SUCRALOSE 0.01%-5%  VITAMINA PALMITATE- 15% 0.01%-10% PYRIDOXINE HYDROCHLORIDE - 82.3% 0.01%-10%(VITAMIN B6) RIBOFLAVIN - 100% (Vitamin B2) 0.01%-10% THIAMINEHYDROCHLORIDE - 89.2% 0.01%-10% (Vitamin B1) MAGNESIUM STEARATE0.01%-2%  SILICA 0.01%-2%  GLYCERYL MONOOLEATE 0.01%-1%  5% VITAMIN K -100% 0.01%-5%  2.5% VITAMIN D3 LIQUID - 100% 0.01%-5%  BUTYLATEDHYDROXYTOLUENE 0.01%-1%  CYANOCOBALAMIN - 100% (Vitamin B12) 0.001%-1% 

Films identified in Table 2 above as “Zinc/Elderberry” contain thefollowing components listed in Table 10: TABLE 10 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-60% ZINC GLUCONATE 0.01%-20%ELDERBERRY EXTRACT 0.01%-20% FRUCTOSE 0.01%-20% NATURAL & ARTIFICIALFLAVORS 0.01%-30% POLYETHYLENE OXIDE 0.01%-20% POLYDEXTROSE 0.01%-20%ASCORBIC ACID - 100% (Vitamin C) 0.01%-20% SUCRALOSE 0.01%-5%  GLYCERYLMONOOLEATE 0.01%-1%  MAGNESIUM STEARATE 0.01%-5%  TITANIUM DIOXIDE0.01%-2%  SILICA 0.01%-2%  BUTYLATED HYDROXYTOLUENE 0.01%-1% 

Films identified in Table 2 above as “B-Complex Vitamin” contain thefollowing component listed in Table 11: TABLE 11 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-60% POLYETHYLENE OXIDE 0.01%-50%CALCIUM d-PANTOTHENATE -92% (Vitamin 0.01%-20% B5) POLYDEXTROSE0.01%-30% NATURAL &ARTIFICIAL FLAVORS/FLAVOR 0.01%-25% ADJUVANTSPYRIDOXINE HYDROCHLORIDE -82.3% 0.01%-20% (VITAMIN B6) RIBOFLAVIN -100%(Vitamin B2) 0.01%-20% THIAMINE HYDROCHLORIDE -89.2% 0.01%-20% (VitaminB1) SUCRALOSE 0.01%-5%  PROPYLENE GLYCOL 0.01%-5%  MAGNESIUM STEARATE0.01%-10% SILICA 0.01%-2%  GLYCERYL MONOOLEATE 0.01%-1 % BUTYLATEDHYDROXYTOLUENE 0.01%-1%  DYE 0.01%-1%  CYANOCOBALAMIN -100% (VitaminB12) 0.001%-1% 

Films identified in Table 2 above as “Immune Booster” contain thefollowing components listed in Table 12: TABLE 12 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-70% POLYDEXTROSE 0.01%-50%POLYETHYLENE OXIDE 0.01%-50% ZINC CITRATE TRIHYDRATE 0.01%-40% SUCRALOSE0.01%-5%  NATURAL FLAVORS 0.01%-20% CITRIC ACID 0.01%-20% MAGNESIUMSTEARATE 0.01%-10% SILICA 0.01%-2%  SODIUM CITRATE 0.01%-5%  GLYCERYLMONOOLEATE 0.01%-1%  BUTYLATED HYDROXYTOLUENE 0.01%-2%  MONOAMMONIUMGLYCYRRHIZINATE 0.01%-1%  DYE 0.01%-1% 

Films identified in Table 2 above as “Cold & Cough” contain thefollowing components listed in Table 13: TABLE 13 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-60% POLYDEXTROSE 0.01%-30% NATURAL&ARTIFICIAL FLAVORS 0.01%-25% POLYETHYLENE OXIDE 0.01%-50% ASCORBIC ACID-100% (Vitamin C) 0.01%-30% ZINC CITRATE DIHYDRATE 0.01%-20% ECHINACEAPURPUREA 0.01%-20% SUCRALOSE 0.01%-10% PECTIN 0.01%-20% CITRIC ACID0.01%-10% SODIUM CITRATE 0.01%-5%  MAGNESIUM STEARATE 0.01%-10% SILICA0.01%-2%  GLYCERYL MONOOLEATE 0.01%-1%  DYE 0.01%-1%  BUTYLATEDHYDROXYTOLUENE 0.01%-1%  MONOAMMONIUM GLYCYRRHIZINATE 0.01%-1% 

Films identified in Table 2 above as “Stress Relief” contain thefollowing components listed in Table 14: TABLE 14 Component Weight %HYDROXYPROPYL METHYLCELLULOSE 0.01%-60% CHAMOMILE 0.01%-40% PASSIONFLOWER 0.01%-40% PECTIN 0.01%-20% NATURAL &ARTIFICIAL FLAVORS 0.01%-25%GLYCERIN 0.01%-10% POLYSORBATE 80   0%-2% SUCRALOSE 0.01%-5% POLYDIMETHYLSILOXANE EMULSION 0.01%-2%  ASPARTAME 0.01%-5%  POTASIUMACESULFAME 0.01%-3%  POTASSIUM SORBATE 0.01%-1% 

Films identified in Table 2 above as “Cinnamint” contain the followingcomponents listed in Table 15: TABLE 15 Component Weight % HYDROXYPROPYLMETHYLCELLULOSE 0.01%-70% POLYETHYLENE OXIDE 0.01%-50% POLYDEXTROSE0.01%-30% BUTYLATED HYDROXYTOLUENE 0.01%-1% GLYCERYL MONOOLEATE0.01%-1%  MAGNESIUM STEARATE 0.01%-10% SILICA 0.01%-2%  POTASSIUMSORBATE  0.01%-0.1% SODIUM BENZOATE  0.01%-0.1% NATURAL &ARTIFICIALFLAVORS 0.01%-30% SUCRALOSE 0.01%-5%  XYLITOL 0.01%-10% DYE 0.01%-1% 

Films identified in Table 2 above as “Dextromethorphan Hydrobromide”contain the following components listed in Table 16: TABLE 16 ComponentWeight % Dextromethorphan Hydrobromide 60% 0.01%-60% POLYETHYLENE OXIDE0.01%-70% POLYDEXTROSE 0.01%-30% HYDROXYPROPYL METHYLCELLULOSE 0.01%-70%NATURAL &ARTIFICIAL FLAVORS 0.01%-30% SUCRALOSE 0.01%-5%  MAGNESIUMSTEARATE 0.01%-10% SILICA   0%-2% SODIUM BICARBONATE 0.01%-5%  XANTHANGUM 0.01%-10% TITANIUM DIOXIDE 0.01%-5%  BUTYLATED HYDROXYTOLUENE0.01%-1%  DYE 0.01%-1% 

The films prepared in these Examples exhibited improved glidantproperties, particularly the ability to slide against one anotherwithout sticking together.

Examples 244- 300

Water-soluble thin films were prepared incorporating silica andmagnesium stearate as anti-tacking agents in the amounts described inTable 17. More specifically, various combinations of silica andmagnesium stearate were incorporated into a variety of different filmcompositions as shown in the table below. TABLE 17 Magnesium Silica¹stearate (weight Example Film description (weight %) %) 244 SOURS 1.52.5 245 ENERGY/WELLNESS 0.75 1 SUPPLEMENT² 246 ENERGY/WELLNESS 0.75 1SUPPLEMENT² 247 MELATONIN 1 2 248 MELATONIN 1.5 1.5 249 CHLORINE DIOXIDE1.5 1.5 250 MELATONIN 1.5 1.5 251 MELATONIN 1.5 1.5 252 MELATONIN 1.51.5 253 MELATONIN 1.5 1.5 254 CHLORINE DIOXIDE 1.5 1.5 255 MELATONIN 1.11.3 256 MULTIVITAMIN 1 1 257 MULTIVITAMIN 1 1 258 B COMPLEX VITAMIN 1 1259 MULTIVITAMIN 1 1 260 B COMPLEX VITAMIN 1 1 261 COLD & COUGH 1 1 262MULTLVITAMIN 1 1 263 MULTIVITAMIN 1 1 264 MULTIVITAMIN 1 1 265MULTIVITAMIN 266 MULTIVITAMIN 267 MULTIVITAMIN 268 MULTIVITAMIN 1 1.5269 IMMUNE BOOSTER 1.16 1.16 270 MULTIVITAMIN 1 1 271 ENERGY/WELLNESS 11.5 SUPPLEMENT² 272 MULTIVITAMIN 1 1.5 273 MULTIVITAMIN 1 1.5 274MELATONIN 1.1 1.3 275 MULTIVITAMIN 1 1 276 MULTIVITAMIN 1 1 277MULTIVITAMIN 1 1 278 MULTIVITAMIN 1 1 279 MULTIVITAMIN 1 1 280ENERGY/WELLNESS 1.5 1.5 SUPPLEMENT² 281 MULTIVITAMIN 1 1.5 282MULTIVITAMIN 1 1.5 283 MULTIVITAMIN 1.5 0.3 284 MULTIVITAMIN 1 1 285B-COMPLEX VITAMIN 1 1 286 ENERGY/WELLNESS 1 0.5 SUPPLEMENT² 287MULTIVITAMIN 1 1 288 MELATONIN 1.1 1.3 289 B-COMPLEX VITAMIN 1 1 290B-COMPLEX VITAMIN 1 1 291 ENERGY/WELLNESS 1 0.5 SUPPLEMENT² 292ENERGY/WELLNESS 1 0.5 SUPPLEMENT² 293 B-COMPLEX VITAMIN 1 1 294MULTIVITAMIN 1 1 295 CHLORINE DIOXIDE 1.5 1.5 296 MULTIVITAMIN 1 1.5 297MULTIVITAMIN 1 1 298 MULTIVITAMIN 1 1 299 MULTIVITAMIN 1 1 300BENZOCAINE/MENTHOL 1.5 1.5¹Sipernat 500LS, available from Degussa²Energy/Wellness Supplement may contain any/all of the following activesor combinations thereof: Green Tea, Guarana, Chromium Picolinate,Caffeine, Yohimbie HCl, Taurine, Vitamin B3, Vitamin B6, Vitamin B12

Besides silica and magnesium stearate, the remainder of the componentscontained in the films listed in Table 17 are provided in connectionwith Table 2 above. The film descriptions used in Tables 2 and 17 arethe same.

The films prepared in these Examples exhibited improved glidantproperties, particularly the ability to slide against one anotherwithout sticking together.

While there have been described what are presently believed to be thepreferred embodiments of the invention, those skilled in the art willrealize that changes and modifications may be made thereto withoutdeparting from the spirit of the invention, and it is intended toinclude all such changes and modifications as fall within the true scopeof the invention.

1. An edible film for delivery of an active comprising: an edible, water-soluble polymer; at least one anti-tacking agent selected from the group consisting of lubricants, antiadherants, glidants and combinations thereof; and an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof, wherein said film is self-supporting.
 2. The film of claim 1, wherein said anti-tacking agent comprises Vitamin E TPGS.
 3. The film of claim 1, wherein said anti-tacking agent comprises magnesium stearate.
 4. The film of claim 3, wherein said anti-tacking agent further comprises silica.
 5. The film of claim 1, wherein said anti-tacking agent is present in amounts of about 0.01% to about 20% by weight of said delivery system.
 6. The film of claim 1, wherein said anti-tacking agent comprises: magnesium stearate present in amounts of about 0.1% to about 2.5% by weight of said delivery system; and silica present in amounts of about 0.1% to about 1.5% by weight of said delivery system.
 7. The film of claim 1, wherein said water-soluble polymer comprises polyethylene oxide and a cellulosic polymer.
 8. The film of claim 7, wherein said cellulosic polymer comprises hydroxypropyl cellulose.
 9. The film of claim 7, wherein said cellulosic polymer comprises hydroxypropylmethyl cellulose.
 10. The film of claim 1, wherein said active component comprises dextromethorphan.
 11. The film of claim 1, further comprising polydextrose.
 12. The film of claim 1, wherein said film is applied to an oral cavity of a mammal.
 13. The film of claim 13, wherein said film adheres to the tongue of the mammal.
 14. An edible film for delivery of an active comprising: an edible, water-soluble polymer component comprising at least one polymer selected from the group consisting of hydroxypropyl cellulose, hydroxypropylmethyl cellulose, polyethylene oxide and combinations thereof; an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof; and an anti-tacking agent comprising Vitamin E TPGS present in amounts of about 0.01% to about 20% by weight of said film.
 15. An edible film for delivery of an active comprising: an edible, water-soluble polymer component comprising polyethylene oxide in combination with a polymer selected from the group consisting of hydroxypropyl cellulose, hydroxypropylmethyl cellulose and combinations thereof; and Vitamin E TPGS present in amounts sufficient to provide anti-tacking and therapeutic properties, wherein said film is self-supporting.
 16. An edible film for delivery of an active comprising: an edible, water-soluble polymer comprising polyethylene oxide and hydroxypropyl cellulose; polydextrose, wherein said polyethylene oxide, hydroxypropyl cellulose and polydextrose are present in a ratio of about 45:45:10; an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof; and at least one anti-tacking agent.
 17. An edible film for delivery of an active comprising: (a) a self-supporting film having at least one surface, said film comprising: (i) an edible, water-soluble polymer; and (ii) an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof; and (b) a coating on said at least one surface of said self-supporting film, said coating comprising at least one anti-tacking agent.
 18. A multi-layer film for delivery of an active comprising: (a) at least one first film layer comprising: (i) an edible, water-soluble polymer; and (ii) an anti-tacking agent; and (b) a second film layer comprising: (i) an edible, water-soluble polymer; and (ii) an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof, wherein said first film layer is substantially in contact with said second film layer.
 19. The multi-layer film of claim 18, wherein said first film layer is laminated to said second film layer.
 20. A process for making a self-supporting film having a substantially uniform distribution of components comprising: (a) combining an edible, water-soluble polymer, a solvent, an active component selected from the group consisting of cosmetic agents, pharmaceutical agents, vitamins, bioactive agents and combinations thereof and at least one anti-tacking agent to form a matrix with a uniform distribution of said components; (b) forming a self-supporting film from said matrix; (c) providing a surface having top and bottom sides; (d) feeding said film onto said top side of said surface; and (e) drying said film by applying heat to said bottom side of said surface.
 21. The process of claim 20, wherein said anti-tacking agent comprises Vitamin E TPGS.
 22. The process of claim 20, wherein said anti-tacking agent comprises magnesium stearate and silica.
 23. The process of claim 20, wherein said matrix further comprises polydextrose.
 24. The process of claim 20, wherein said film is ingestible.
 25. The process of claim 20, wherein said film is flexible when dried.
 26. The process of claim 20, wherein step (e) comprises applying hot air currents to said bottom side of said surface with substantially no top air flow. 